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Seiko Ruputer was the first worlds smart watch invented in 1998. Smart watch is a touch screen wristwatch which can be connected to a phone through Bluetooth or WiFi, its function is more than time like mostly used for tracking the fitness. It includes pedometer that counts the number of steps walked throughout the day. Also have monitors heart rate while exercises. In short, smart watch have health and fitness tool like ECG monitors, Blood pressure monitor etc. It is not only the source of tracking fitness but best gadget for entertainment like can play music with or without smart phone. Smart watch has become fashion piece enhances the personality of the wearer.A smart watch is a wearable computing device that closely resembles a wristwatch or other time-keeping device. From 23 May 2018, the Bureau of Indian Standards (BIS) has required SMART WATCHES to be registered as per IS 13252 (Part 1):2010 underCompulsory Registration Schemefrom BIS. No domestic as well as foreign manufacturer can sell smart watch in Indian market.
The first electric clock was invented by Alexender Bain in 1841. An electronic clock is the clock that is powered by electricity. And these clocks mostly display the time, and in addition to this, some clocks have a feature to display the temperature also digitally. Digital clocks use an electronic gear mechanism which is known as the counter. It uses displays like LED (Light-emitting Diodes) and LCD (Liquid crystal display) to display the time. It is known as the 7-segmented display because it uses 7 segments that can light up to the display a number. In short, Electronic Clock is powered by electricity. Electronic Clock with Mains Power is under the safety of household and similar electrical appliances. BIS has covered only digital electric clock which works with the electricity and shall have digital feature.
Pisen is the inventor of Power Bank. Power Bank has become the necessary Gadget for everyone. It is the portable battery-powered device for charging electronic devices when you are on the go. It used to charge mobile phones, tablets, speakers, and also laptop depends upon its capacity. The power bank comes in different sizes and in a different color, totally portable, not too heavy. You can take it anywhere with you and enjoy your trip. One excellent feature is that it has multiple charging ports, where you can charge various gadgets at the same time. It has overcome the drawback of mobile or other gadgets battery failure. In short, Power banks are portable batteries that use circuitry to control any power in and power out. From 13 May 2015, the Bureau of Indian Standards (BIS) has required POWER BANK to be registered as per IS 13252 (Part 1):2010 under the Compulsory Registration Scheme from BIS. The Government of India has taken this step to just ensure that this device is safe for public health. Power Bank contains lithium ion battery which is very hazardous that is why its quality should be good.
Day by day, Bluetooth connectivity has become a trend. Now we can connect most of the devices with each other without using wires. The major function of Bluetooth in the speaker is that it receives digital audio wirelessly by Bluetooth protocol when it is paired with Bluetooth. Bluetooth speakers accept digital audio by Bluetooth wireless transmission. Firstly, convert the analog audio, amplify it, and at last convert it into the sound through the speaker. Today, most portable speakers use Bluetooth technology. A Bluetooth speaker is, without a doubt, the most adaptable speaker you can possess. You have a simple and effective approach to get music whenever and wherever you need it. Bluetooth speakers can send full-range audio into any room in your house for a reasonable price and without taking up much space. In short, Bluetooth speaker is an electronic device which is used for amplification of voice, and it is provided connectivity with smartphones, tablets, I pad, laptops and Computers, and it also increases the audio through the built-in speakers.
A plotter is like a printer that is used to print vector graphics or graphical output on paper. Remington-Rand invented the plotter in 1953 and used it with the UNIVAC computer to create technical drawings. The printer use tonner but at the same time plotter uses a pen, pencil, marker, or other writing tools to draw many continuous lines onto the paper. It helps in producing the hard copy as it works on large sheets while maintaining high resolution. Plotters are mostly used by the printing companies to print large media materials like printer banners, large posters, wallpapers, architectural drawings like blueprints etc. All types of plotters are mandatory under the BIS Compulsory Registration Scheme. From 3rd July 2013, the Bureau of Indian Standards (BIS) has required PLOTTERS to be registered as per IS 13252 (Part 1):2010 under the Compulsory Registration Scheme from BIS. It is compulsory for domestic and foreign manufacturers to get their plotters registered with BIS Registration online to sell in the Indian market.
A wireless microphone is also known as the cordless microphone, mostly used in television broadcasting, the entertainment industry, and public speaking so that person can move freely without using cables. It is directly connected to the sound recording or amplifying equipment. It has a small radio transmitter that transmits the audio signals from the microphone to the near receiver in the form of audio. It uses the VHF or UHF frequency band and allows the users voice transmitted wirelessly. In short, a wireless microphone is used for sound recording without a physical cable that is connected to amplifying equipment. On 01 April 2021, the Bureau of Indian Standards (BIS) has ordered the Wireless Microphone to be registered under the Compulsory Registration Scheme from BIS under the Gazette of India. BIS registration online is compulsory for domestic manufacturers and foreign manufacturers who want to sell their wireless microphone in Indian.
The storage battery is also known as the solar storage battery. Its major function is to contribute to the electricity supply even when the sun is not shining. The term "storage" refers to systems that can catch electricity, store it as another type of energy (chemical, thermal, or mechanical), and then release it when needed. The best of solar and storage is they provide backup power during an electrical disruption. In short, the solar panel collects the solar energy from the sun and converts it into electricity. A solar storage battery is a system that is charged by a connected solar system, such as photovoltaic. Manufacturers of storage batteries are required to have registration from BIS under a compulsory registration scheme. As per the Government of India, a manufacturer cannot manufacture or store goods for selling purposes, import, or distribute which do not conform to the Indian Standard IS 16270:2014.
Mail processing machine is mostly used in post office department. The post office department was using mostly old fashion methods, which were very expensive and inefficient; mails were done by hand. Keeping this in consideration and to increase the efficiency and accuracy of the post office department mail processing machine was introduced. BIS cover all kinds of Mail Processing Machines/Postage Machines/Franking Machines. A franking machine, sometimes known as a 'Postage Meter, ' is a device that prints a barcode on a letter or delivery instead of a traditional stamp. A franking machine can download and securely store postage dollars, and it can also help the user choose mail classes and special services. These machines need to get BIS Registration before being sold, exported/imported to the Indian Market. On 13 May 2015, the Bureau of Indian Standards (BIS) has required MAIL PROCESSING MACHINE to be registered as per IS 13252 (Part 1):2010 under Compulsory Registration Scheme from BIS.
Power adaptors are also known as the plug pack, plug-in adaptor, adaptor block, line power adaptor, and domestic main adaptor. It is the electronic device considered as the source of input or power supply to the device. Power adaptors present in the market are used to power supply to both direct current DC and alternate current AC devices. These come in different output voltage ratings. A power adapter is one of the great deals for audio, video, and similar electronic apparatus. As a power adaptor is an electronic device mostly used in every home, keeping this in consideration, the Government of Indian and Bureau of Indian Standards has taken a step that it is compulsory for the manufacture to register his product under Compulsory registration scheme as per IS 616.
Portable computers are in high demand these days, and the major reason behind this is their lightweight and flexibility. You can carry them wherever you want. A wide range of portable computers like a notebook, tablet PC, etc., has come into the market with different features in different brands. Notebooks/ tablet PC has made life very easy and also save a lot of time. These come with a battery and AC-power adapter, also known as a personal computer or laptop. Notebooks/tablets are mostly of high cost and most used devices in the market, keeping this in consideration, BIS Bureau of Indian Standards on 3rd July 2013, has made compulsory to register notebook/tablet PC as per Indian Standard IS 13252 (Part 1): 2010 under Compulsory Registration Scheme.
Headphones were created in the 1880s, but not the headphones you're thinking of; these headphones weighed 10 pounds and had less to do with music. These are more akin to phones. Stereo head phone using Bluetooth was invented in 2004. Today, we see many people are using wireless headphone or earphone to play music, watch videos and talk on the photo. You are certain to realize the benefits of headphones whether you go jogging, travel to school or work, or simply want to enjoy the highest quality sound without any background noise. Wireless Headphone and Earphone is a pair of small loudspeakers worn on around the head over a users ears for listening voice. From 01 April 2021, the Bureau of Indian Standards (BIS) has requiredthe True Wireless (TWS) Earphones, Wireless Headphone, TWS Earbuds, and Wireless Neckbandsto be registered as per IS 616: 2017 under Compulsory Registration Scheme from BIS. The major motive of covering wireless headphone and earphone is to safeguard the human health as it can damage the hearing sense of human being.
First, the hard disk was invented in 1957 as a component of the IBM 305 RAMAC system. A hard disk drive is the portable electromechanical data storage device; you can use it to store your computer data. The external hard disk comes with a USB which connects the hard disk with a computer or other telecommunication devices and can easily transfer the data from the computer to the hard disc and vice versa. Hard disk drive comes in different storage capacities. Mostly hard disk drive is used for storing old photos or videos, Records and archival data, completed projects etc., and it is the best option to it as a backup device. The biggest advantage of having an external drive is that it is highly portable - it can be linked to several computers and allows you to take a huge quantity of storage with you no matter where you are. On 01 April 2021, the Bureau of Indian Standards (BIS) has required the USB Type External Hard Disk Drive to be registered as per IS 13252: 2010 under the Compulsory Registration Scheme from BIS.
Emergency lighting refers to light sources that are battery-powered or otherwise independently powered and are meant to operate when a power loss causes low visibility in the workplace. Emergency lighting units are now extensively used to provide lighting in an emergency for the set period, allowing routine operations to continue or be terminated safely in the event of a power outage. In the event of a power outage or restoration of regular power, an automated switching mechanism is usually supplied to turn on/off the emergency lighting units. Emergency lighting uses an electric lamp, charging, accumulator, and other devices for operating in case of need. Most new buildings now have emergency lighting installed during construction. On 23 May 2018, the Bureau of Indian Standards (BIS) has required EMERGENCY LIGHTING to be registered as per IS 10322 (PART 5): SECTION 8: 2013 under Compulsory Registration Scheme from BIS. BIS Certification is compulsory for both Indian as well as foreign manufacturers, without BIS Registration, no manufacturer can manufacture, import/export, store or sell the emergency lighting.
LED lighting chain is the best way to illuminate the home with happiness. Whether its home decoration, office decoration, garden decoration, tree decoration, or stair railing decoration LED lighting chain is the best to make things more beautiful. It brightens your home; it can be used both inside and outside the home. I must say you can use it where you want to create the environment of happiness. It comes in different designs, colors, and lengths. LED Lighting Chains transform the mood of the environment with a warm glow and brightens up forgotten corners of your home. On 23 May 2018, the Bureau of Indian Standards (BIS) has required LED LIGHTING CHAINS to be registered as per IS 10322 (PART 5): SECTION 7:2013 under Compulsory Registration Scheme from BIS.
An adaptor is an electronic device that is used to connect any household & similar electrical appliances to a power supply or for connecting different devices of electrical and electronic equipment together. Power Adapter is also known as the plug pack, plug-in adapter, line power adapter, domestic main adapter, adapter block, etc., and it is a sort of external power supply. It changes the characteristics of one electrical gadget to those of another, otherwise unsuitable device or system. From 23 May 2018, the Bureau of Indian Standards (BIS) has required ADAPTORS FOR HOUSEHOLD AND SIMILAR ELECTRICAL APPLIANCES to be registered as per IS 302 (Part 1):2008 under Compulsory Registration Scheme from BIS. If your products are registered under the BIS, then you can easily import/export, manufacture, and sell power adapters hassle-free in India Market.
LED stands for Light-emitting Diodes. LED Bulb technology is really great as it saves 90% energy and lasts for more than 60000 hours. LED bulbs are unbreakable, cool to touch, and saves both money and the environment in the best way. The blast word seems odd, but it is the heart of the fluorescent bulb and is also called the driver. The word "self-ballasted" simply indicates that the bulb does not need a ballast to control the flow of energy. Self-ballasted CFL light bulbs are self-contained and may be screwed in the same way as standard incandescent bulbs are. Self-ballasted CFLs are the current go-to for standard lighting requirements as they are simple and convenient. In short, a blast controls the current that flows through a light. It provides an initial burst to get things started and then ensures that the electric current is regulated and constant.
LED Street light uses light-emitting diodes as its light source and also known as the street lamps, illuminate roadways, parking lots, sidewalks, etc. Streetlights are used to illuminate roads, junctions, street corners, and other public places such as alleys, parks, and walkways across the world. Streetlights offer illumination to improve visibility, enhance road safety for cars and pedestrians, and deter theft or violence. Previously, street light management was accomplished by centralized control of the entire region or line. People's awareness of energy-saving and environmental preservation has increased, and this has resulted in new regulations for the control of street lighting. The control now needs precise control in order to gain control of all lights. It must not only be able to manage the state of the street light, but it must also comprehend the functioning status of a specific street light.On 23rd May 2018, the Bureau of Indian Standards (BIS) has required a Street light to be registered as per IS 10322 (Part 5) under the Compulsory Registration Scheme from BIS. No domestic or foreign manufacturer shall manufacture, export to India, store, distribute or sell the sealed secondary cells in the Indian Market.
The Lamp was discovered at least as early as 70, 000 BCE. But with the rapid advancement of technology, lamps have come in different designs, styles, and updated technology. LED hand lamps are useful in an emergency situation, automotive work inspection, camping, etc. it uses Light-emitting diodes. LED hand lamps come in different designs with long cables. These lamps mostly save energy and are shockproof. LED hand lamps come with an inbuilt battery or with wire or with both wires as well as battery. But under BIS, only an LED lamp with cable is covered. It is compulsory to obtain the BIS certification for LED Hand Lamps in order to manufacture, sell, distribute, import/export, and store the LED hand lamp. In short, Led Hand Lamps are the ideal solution for when the fixed on-site lighting system does not provide sufficient light for your needs.
A wireless keyboard is the solution to work comfortably on your computer as well as your laptop. The major function of the keyboard is to help users to communicate with a laptop, computer, tablets etc., with the aid of Radiofrequency like WiFi, Bluetooth or infrared (IR) technology etc. Most keyboards use light waves to transmit signals; otherwise can connect with Bluetooth. The keyboard is an input device that is the way to increase productivity. Wireless technology is really cool and more convenient because the absence of wires really helps in organizing the workplace better. The wireless computer also comes under the BIS RegistrationCompulsory Registration Scheme. The BIS Registration is a trusted tag in itself because it indicates that the product is safe for the public, as it has passed through various tests.
Recessed LED Luminaries are the LED light fixture which is installed into the hollow opening of the surface whether its on the ceiling or on another surface. It includes 3 main fixtures that are bulb, trim, and housing. The housing is the majority of the fixture that is buried within the wall or ceiling and houses the fixture's electrical connections. Trim refers to the attractive, visible component of the fixture, which may incorporate baffles, reflectors, or shades. The last component is the bulb, which is the component of the fixture that generates light. The lights are very sleek, easily fit anywhere in less space, and illuminates the whole area. These lights are great for the kitchen, closets, shower stalls, and anywhere there are low ceilings. As recessed lights are electric in nature, so it is compulsory to register recessed LED Luminaries under BIS Registration as per IS 10322 (Part 5/Section 2): 2012 under Compulsory Registration Scheme from BIS. It is compulsory for the domestic as well as the foreign manufacturers to register recessed LED Luminaries under compulsory registration scheme or BIS registration otherwise it will be a punishable offense.
Indoor air quality is a crucial aspect of our health and well-being, especially in a world where we spend most of our time indoors. As a result, many individuals and organizations are taking steps to ensure that the products and materials we use in our indoor spaces are safe and have low chemical emissions. This is where Green Guard Certification comes in. In India, this certification has become increasingly popular, allowing manufacturers to create and buyers to identify products that meet strict environmental standards. Let’s explore the importance of Green Guard Certification and how it’s helping to create a safer and healthier indoor environment in India.
I. Introduction
Brief explanation of Green Guard Certification
Green Certification is a rigorous program that products for low chemical emissions. This program is designed to ensure that products do not cause indoor air pollution and contribute to harmful effects on human health. The certification is conducted by the Greenguard Environmental Institute, which is a non-profit organization recognized globally. The program has two tiers of certification: Green Guard and Green Guard Gold. The latter has even higher standards of testing and is recommended for those who are more sensitive to air pollution, such as children or elderly people. The certification process involves testing products in specially-designed testing chambers for up to two weeks, where they are subjected to controlled temperatures and humidity levels. The testing checks for over 10, 000 chemicals and VOC emissions, ensuring that the products meet the strict standards of low emission levels set by the certification program. Obtaining Green Guard Certification shows a manufacturer’s commitment to a healthier environment and can provide a competitive advantage by appealing to consumers who are more health- and environment-conscious.
Significance of the certification in India
Green Guard Certification is becoming increasingly significant in India due to the rapid industrialization and urbanization in the country. The certification ensures that the products or materials used inside buildings have low chemical emissions, which improves the indoor air quality and reduces exposure to harmful chemicals. The certification is especially important for schools, healthcare facilities, and homes, where people spend most of their time indoors. With the rising concern over indoor air pollution and its impact on human health, the certification has become a benchmark of quality for manufacturers in India. Green Guard certification gives Indian manufacturers a competitive edge by enhancing their reputation and promoting their commitment to protecting human health and the environment. Moreover, with the stringent regulations and standards put in place by the government, the certification has become a necessity for manufacturers to ensure that their products comply with the required standards and regulations. In conclusion, Green Guard certification is an important tool for promoting healthier indoor environments in India and building a sustainable future.
The purpose of Green Guard Certification
The purpose of Green Guard Certification is to ensure that products and materials have low chemical emissions that are safe for human health. With the growing concern of indoor air pollution and its impact on human health, Green Guard Certification provides a solution to help improve indoor air quality. By testing products in strict testing chambers, the certification ensures that they emit minimal volatile organic compounds (VOCs) which are harmful chemicals that can lead to respiratory diseases and cancer. Green Guard Certified products also provide manufacturers with a competitive advantage, as they demonstrate their commitment to sustainability and health.
ISO 31000 provides principles and generic guidelines to assist organizations in establishing, implementing, operating, maintaining and continually improving their risk management framework.
It is not specific to any industry or sector, so it can be used by any public, private or community enterprise, association, group or individual. This standard can be applied throughout the life of an organization, and to a wide range of activities, including strategies and decisions, operations, processes, functions, projects, products, services and assets.
This standard is not intended to promote uniformity of risk management across organizations. The design and implementation of risk management plans and frameworks will need to take into account the varying needs of a specific organization, its particular objectives, context, structure, operations, processes, functions, projects, products, services, or assets and specific practices employed.
ISO 31000 is organized into the following main clauses:
Clause 3: Principles
Clause 4: Framework
Clause 5: Process
Each of these key activities is listed below.
Clause 3: Principles of risk management
In order to have an effective risk management, an organization has to comply with these 11 principles.
Clause 4: Framework
ISO 31000 states that the success of risk management will depend on the effectiveness of the management framework providing the foundations and arrangements what will embed it throughout the organization at all levels.
The framework:
This clause describes the necessary components of the framework for managing risk and the way in which they interrelate in an iterative manner.
Design of framework for managing risk: Before the implementation, the organization must design a framework for managing risk. This includes:
ISO 31000 states that the success of risk management will depend on the effectiveness of the management
Our ISO 14855-1:2012 Certification Consultancy Service ensures a streamlined process for environmental biodegradability testing. Our expert consultants guide your organization through the certification requirements, offering comprehensive assistance in protocol implementation, documentation, and audit preparation. We focus on aligning your practices with ISO 14855-1 standards, emphasizing environmentally responsible practices. Our service encompasses detailed training sessions, documentation review, and continuous support to guarantee a successful certification process. By choosing our consultancy, you gain a partner dedicated to enhancing your environmental footprint and ensuring compliance with ISO 14855-1:2012, fostering a commitment to sustainable and eco-friendly practices within your business.
FCC Certification ServicesWhat is FCC Certification?
The United States has required standards for products that might contribute to electromagnetic interference in order to reduce the level of radio frequency (rf) interference between electronic devices. Any electronic device or piece of equipment that is sold in the United States must not compromise the safety of the American public or interfere with other electronic products.The Federal Communications Commission (FCC) is in charge of the development, enforcement and implementation of regulations that Congress set forth in the Communications Act of 1934 and the Telecommunications Act of 1996. The FCC is an agency of the United States federal government that was created to regulate all forms of telecommunication inside of the U.S. including radio, television, digital cameras, Bluetooth, wireless devices and a broad gamut of RF electronics.When an electronic device has an FCC certificate, it means the product has been tested to comply with FCC standards and it has been approved. An FCC certification does not imply that the product is safe or durable. It simply means that it meets regulated limits for ionizing radiation. A certification does not imply that the device was manufactured any specific way. FCC approval can be granted as long as the electronic device meets FCC emission rules and regulations and has been tested to comply with FCC standards.
Compliance testing and requirements set by the Federal Communications Commission can seem extremely confusing. They can cause major frustration for manufacturers and electronic distribution companies. We can help your company better understand the process needed to gain an FCC certificate and help your product become certified to be sold in the United States.
What Products Require an FCC Certificate?
Radio frequency (RF) equipment that is sold or distributed in the United States is required to undergo testing in order to stay in compliance with standards set by the Federal Communications Commission under the EMC directive. Testing limits both intentional and unintentional electromagnetic radiation that is emitted from RF equipment in order to keep users safe. CSIA can help your company gain an FCC certificate for various types of RF emitting devices, including, but not limited to:
What are FCC Regulations?
Federal Communications Commission standards depend on the type of radio frequency emitting device that is being tested. The FCC has come up with categories that identify what type of regulations and testing are necessary for different devices to obtain certified authorization for distribution. Testing is broken up into product categories including FCC Part 11, FCC Part 15, Part 18, Part 22, Part 24, Part 68, Part 90 and FCC Part 95. One of the most common types of device approval is for FCC part 15 certification, which refers to regulations set for television receivers.
ISO 9001:2015
ISO 9001 is a globally recognized standard for quality management. It helps organizations of all sizes and sectors to improve their performance, meet customer expectations and demonstrate their commitment to quality. Its requirements define how to establish, implement, maintain, and continually improve a quality management system (QMS).
Implementing ISO 9001 means your organization has put in place effective processes and trained staff to deliver flawless products or services time after time.
Why is ISO 9001 important?
With more than one million certificates issued to organizations in 189 countries, ISO 9001 is the most widely used quality management standard in the world. Within the ISO 9000 family, which defines seven quality management principles including a strong customer focus and continual improvement, ISO 9001 is the only standard that can be certified to (though certification is not mandatory).
Business benefits include:
Benefits of ISO 9001
What is GDP certification?
The abbreviation GDP stands for Good Distribution Practices and refers in this context to the storage and transport of finished medicinal products and active ingredients.
Manufacturers of pharmaceutical products are subject to the requirements of Good Manufacturing Practices (GMP). Manufacturer quality must be ensured throughout the entire supply chain. Even slight fluctuations in temperature and humidity can affect the life and mode of action of medicines. As valuable commodities, pharmaceuticals must also be protected from theft and the introduction of counterfeit drugs into the supply chain.
GDP certification covers areas of the product lifecycle of healthcare products, particularly human pharmaceuticals and active ingredients, that arise around storage and transportation activities. A GDP compliance audit examines the sum of requirements or measures in the distribution chain that ensure the quality and integrity of pharmaceuticals.
Advantages of GDP certification
A GDP certificate identifies your company as a competent and reliable partner for pharmaceutical logistics.
The issuance of GDP certificates is regulated differently in the federal states and is partly only issued to manufacturers and distributors. Federal presidia do not consistently issue certificates to logistics companies. However, pharmaceutical manufacturers and distributors are obliged to monitor their logistics service providers. Individual customer audits involve a great deal of effort for both sides.
With the GDP audit, GUTcert helps logistics service providers to improve their performance and to communicate good distribution practices to their customers. In doing so, we commit ourselves to apply the recognized rules from our accredited ISO processes to the compliance audits against the GDP guidelines.Costs GDP certification
The costs for a certification according to GDP depend on the activities, the number of sites and the size of the workforce. We will be happy to provide you with an individual offer over a 3-year cycle.
Within the framework of integrated audits, synergies can be generated and audit time expenditures and thus costs can be reduced.In addition to your certificate, you will also receive our digital certification marks following the audit, which you can use free of charge for your corporate communications.
Three years after (initial) certification, a recertification audit is carried out. In advance, we will provide you with an effort update.
Good Distribution Practices (GDP) Certification for Pharmaceuticals demonstrates your dedication to good distributive practices and quality in every aspect of your service.
Good Distribution Practices (GDP) is a quality system for warehouse and distribution centers dedicated for medicines. Internationally accepted pharmaceutical GDP regulations stipulate that distributors of pharmaceutical products must align their operations with the standards. The scheme ensures that consistent quality management systems are in place throughout your entire supply chain, from the early delivery of raw materials to the manufacturing plants, to the final shipment of finished drugs to the end user. An independent assessment of compliance against international GDP requirements is the most effective way to establish that your quality management system aligns with GDP guidance.
ISO 22000:2018
This document specifies requirements for a food safety management system (FSMS) to enable an organization that is directly or indirectly involved in the food chain:
a) to plan, implement, operate, maintain and update a FSMS providing products and services that are safe, in accordance with their intended use;
b) to demonstrate compliance with applicable statutory and regulatory food safety requirements;
c) to evaluate and assess mutually agreed customer food safety requirements and to demonstrate conformity with them;
d) to effectively communicate food safety issues to interested parties within the food chain;
e) to ensure that the organization conforms to its stated food safety policy;
f) to demonstrate conformity to relevant interested parties;
g) to seek certification or registration of its FSMS by an external organization, or make a self-assessment or self-declaration of conformity to this document.
All requirements of this document are generic and are intended to be applicable to all organizations in the food chain, regardless of size and complexity. Organizations that are directly or indirectly involved include, but are not limited to, feed producers, animal food producers, harvesters of wild plants and animals, farmers, producers of ingredients, food manufacturers, retailers, and organizations providing food services, catering services, cleaning and sanitation services, transportation, storage and distribution services, suppliers of equipment, cleaning and disinfectants, packaging materials and other food contact materials.
This document allows any organization, including small and/or less developed organizations (e.g. a small farm, a small packer-distributor, a small retail or food service outlet) to implement externally-developed elements in their FSMS.
Internal and/or external resources can be used to meet the requirements of this document.
ISO 22000 sets out the requirements for a food safety management system and can be certified to it. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe. It can be used by any organization regardless of its size or position in the food chain.
ISO 22000 is a food safety management system by the International Organization for Standardization (ISO) which is outcome focused, [1] providing requirements for any organization in the food industry with objective to help to improve overall performance in food safety. These standards are intended to ensure safety in the global food supply chain. The standards involve the overall guidelines for food safety management and also focuses on traceability in the feed and food chain.
Food safety[edit]
Food safety refers to all those hazards, whether chronic or acute, that may make food injurious to the health of the consumer.[2]ISO 22000 standard[edit]
ISO 22000 is the most popular voluntary food safety international standard in the food industry with 51, 535 total number of sites (as per the ISO Survey 2022). The ISO 22000 family are international voluntary consensus standards which align to Good Standardization Practices (GSP)[3] and the World Trade Organization (WTO) Principles for the Development of International Standards.[4] Defining the requirements for a Food Safety Management System (FSMS) and incorporating the following elements which as defined as FSMS principles:
ISO 21001 Certification for Educational Organization Management System (EOMS) provides a framework for establishing flexible, transparent and inclusive classrooms and enables an organization to provide personalized learning to meet the needs and requirements of the individual learner. It helps educational organizations to implement the best practices and aims to improve the quality of education by providing the necessary training to the teachers.
ISO 21001 certification promotes a learner-centric approach and actively engages learners in their own learning. It was published in 2018 by the International Organization for Standardization (ISO) to allow educational institutions to provide high-quality services. It promotes equitable and accessible education for all and offers more personalized learning for learners with special needs and distance learners.
Which Educational Organizations can apply for ISO 21001 Certification?
Any educational organization can apply for ISO 21001 certification, including private and private, regardless of size, nature and location. A list of organizations that can go for ISO 21001 certification for Educational Organization Management System (EOMS) is as follows:
Principles of ISO 21001 Certification
The Educational Organization Management System (EOMS) is not restricted to schools and universities, but organizations that use the curriculum to impart knowledge can apply for ISO 21001 certification. ISO 21001 Certification for Educational Organization Management System (EOMS) follows 11 principles. These are:
ISO 13485 is a crucial international standard designed to enhance the quality management systems of organizations involved in manufacturing medical devices and equipment. This certification outlines stringent control measures to minimize operational errors in the manufacturing process and emphasizes continual improvement in the quality of medical equipment.
Defining Medical Devices
A medical device encompasses instruments, machines, implants, or in vitro reagents used for diagnosing, preventing, or curing diseases or medical conditions. This broad category includes diverse items such as:
Understanding ISO 13485 Certification
ISO 13485 certification is imperative for organizations engaged in designing and manufacturing medical devices and equipment. This certification establishes and maintains a quality management system, ensuring the safety of professionals and patients in clinics, hospitals, and other medical facilities.
ISO 13485 Certification for Businesses
Organizations involved in the design, production, installation, and servicing of medical devices and related services can benefit from ISO 13485 certification. Regulatory authorities and certifying organizations utilize ISO 13485 certification as a baseline for quality assurance during compliance evaluations. This recognition positions certified organizations as reputable and trustworthy providers adhering to international standards of quality and safety.
ISO 13485 Certification Requirements
To achieve ISO 13485 certification, organizations must meet specific standards outlined in the ISO 13485 requirements. These include a review of design controls, development and management of ISO-compliance documentation, quality risk analysis, peer review as evidence of ISO compliance, identification of ISO-mandated documents, an ISO training plan, and internal ISO audits. Adhering to these requirements ensures that organizations meet minimum patient safety, healthcare quality, and regulatory standards.
The ISO 13485 Certification Process
Embarking on the ISO 13485 certification journey involves a structured process designed to assess and validate an organization’s commitment to quality management in medical device manufacturing. The ISO 13485 certification process encompasses several key stages, each integral to achieving certification and demonstrating compliance with ISO 13485 standards.
Benefits of ISO 13485 Certification
The journey begins with the submission of an application for ISO 13485 certification. This initial step involves a comprehensive review of the organization’s details, scope of operations, and specific requirements. A contractual agreement is established, outlining the terms and conditions for the ISO 13485 certification process
What are CMMI Certifications?
CMMI is a popular Process Improvement Framework for organizations. It offers an end-to-end process roadmap for improving the company’s performance and achieving the best outcomes. Organizations that succeed with well-defined business processes receive CMMI certifications. The certification demonstrates their perseverance, efficiency, and capability. These certifications are highly valued and recognized by customers and partners worldwide.
List of Capability Levels
The CMMI Institute grants CMMI certifications as accreditations to global organizations. The certifications have different levels under the Capacity Level and Maturity Level. Here are the primary levels under each of these categories.
Capability levels
a) Capability level 0 represents an organization yet to develop a well-planned practice area.b) Capability level 1 represents an organization that has started improving its operations at the initial level.c) Capability level 2 represents an organization that follows a simple yet effective practice area plan with defined procedures.d) Capability level 3 is for organizations that follow pre-defined industry standards to establish end goals.
Maturity levels
a) Maturity level 0 represents an organization yet to complete a project successfully.b) Maturity level 1 is the initial level, representing an organization that has failed to meet deadlines or targets.c) Maturity level 2 represents an organization stuck with unrelated activities apart from the execution process.d) Maturity level 3 represents an organization that follows a standard approach. This organization overcomes ongoing challenges as per the deadlines.e) Maturity level 4 represents an organization that follows a data-driven approach to meet the end project goals.f) Maturity level 5 represents an organization that has improved continuously. It means that it has adapted to Changes faster and more efficiently.
What is CMMI Maturity Level 3?
It is the third level in the CMMI framework. At this level, organizations have well-defined and documented processes followed by all team members. The focus is improving operations with standardization. Customers and partners highly value CMMI Level 3 certification, indicating the organization has mature processes and can deliver high-quality products and services.
Benefits of CMMI Certification For Customer Satisfaction
a) Improved performance quality: CMMI certification indicates that the organization has well-defined processes. It is capable of providing high-quality solutions.
b) Predictable delivery: CMMI Level 3 certified organizations have matured and well-documented procedures. It ensures that the delivery of products and services is predictable and reliable.
c) Reduced risk: Organizations with CMMI certification have pre-defined processes for risk handling. Hence, the customers gain confidence in believing in them with the desired outcome.
d) Improve efficiency: This certification requires organizations to optimize their operational processes and workflow. It helps to improve overall productivity.
Fundamental Principles to Get CMMI Level 3 Certification
Achieving CMMI Level 3 certification isn’t just a piece of cake. Organizations require to follow certain principles to achieve CMMI Certification.
Establish a process improvement culture
This certification requires organizations to build a unique work culture focusing on continuous improvement. Hence, all team members should be committed to improving processes and eliminating waste.
ISO 45001:2018
ISO 45001 is an international standard that specifies requirements for an occupational health and safety (OH&S) management system. It provides a framework for organizations to manage risks and improve OH&S performance.
The standard establishes criteria for an OH&S policy, objectives, planning, implementation, operation, auditing and review. Key elements include leadership commitment, worker participation, hazard identification and risk assessment, legal and regulatory compliance, emergency planning, incident investigation and continual improvement.
ISO 45001 utilizes the Plan-Do-Check-Act methodology to systematically manage health and safety risks. It applies to organizations of all sizes and can be integrated with other ISO management system standards.
Why is ISO 45001 important?
Implementing ISO 45001 provides significant value to organizations looking to reduce workplace incidents and demonstrate OH&S commitment. Benefits include:
In summary, ISO 45001 enables organizations to better protect their workers and manage OH&S risks, making it an essential standard worldwide.
Benefits
ISO 10002 Customer Satisfaction. Complaints Handling
Manage customer complaints effectively and you’ll have more chance of meeting their expectations as well. And you can quickly turn customer complaints into customer satisfaction instead – especially when you view complaints as an opportunity to improve what you do and how you do it. ISO 10002 can help you to achieve this whatever the size or nature of your business. The customer complaints management system is a basic but essential requirement for any business – especially businesses that want to become and remain successful.
What is ISO 10002 Customer Satisfaction. Complaints Handling?
Customers expect more and more from the service you provide. And your competitors are working harder to meet these expectations. You can too with ISO 10002, the international standard for customer satisfaction. It provides you with guidelines for putting in place your own complaints management system – helping you to identify complaints, their cause and how to eliminate them. ISO 10002 will also allow you to identify areas in your business where you can improve and eventually remove the cause of complaints. The standard outlines management controls and processes that help you to handle customer complaints more effectively and efficiently – making sure that more customers are satisfied with the service you provide.
What are the benefits of customer complaint management?
Implementing ISO 10001 customer complaints management
There are many reasons to work with us to introduce and implement customer complaints management. That’s because we established the first complaints management system standard in 1999 (BS 860). This provided the foundations for the international standard ISO 10002. We can use this experience and knowledge to help you become an expert in managing customer complaints with your own ISO 10002 management system.
Top tips for implementing ISO 10002
An ABMS based on ISO 37001 is intended to help organizations effectively prevent, detect, and respond to bribery. Other forms of corruption, such as fraud, are not covered by the standard. The requirements of the standard are generic and applicable to all organizations, regardless of their type, size, and sector (public, private, or not-for-profit). Furthermore, ISO 37001 can be used to tackle bribery by or of the organization as well as direct and indirect bribery.
SO 37001 follows the High-Level Structure (HLS) and shares the common terminology with other management system standards developed by ISO. This means that an ABMS can either be established as a stand-alone management system, be part of an overall compliance management system based on ISO 37301, or be integrated with other management systems based on standards such as ISO 37002, ISO 9001, and ISO 45001.
ISO 37001 benefits to organizations
Implementing an ABMS based on ISO 37001 can be a good strategic decision to demonstrate an organization’s commitment to effectively prevent, detect, and respond to bribery. Organizations seeking an effective ABMS will have to demonstrate their commitment to prevent bribery by establishing policies, procedures, and controls which contribute in reducing bribery risks. Nevertheless, the requirements of ISO 37001 are generic; therefore, organizations will have plenty of freedom to establish an ABMS which best suits their needs.
Some of the benefits that organizations would obtain by implementing an ABMS based on ISO 37001 include:
ISO 37001:2016 specifies requirements and provides guidance for establishing, implementing, maintaining, reviewing and improving an anti-bribery management system. The system can be stand-alone or can be integrated into an overall management system. ISO 37001:2016 addresses the following in relation to the organization's activities:
· bribery in the public, private and not-for-profit sectors;
· bribery by the organization;
· bribery by the organization's personnel acting on the organization's behalf or for its benefit;
· bribery by the organization's business associates acting on the organization's behalf or for its benefit;
· bribery of the organization;
· bribery of the organization's personnel in relation to the organization's activities;
· bribery of the organization's business associates in relation to the organization's activities;
· direct and indirect bribery (e.g. a bribe offered or accepted through or by a third party).
ISO 37001:2016 is applicable only to bribery. It sets out requirements and provides guidance for a management system designed to help an organization to prevent, detect and respond to bribery and comply with anti-bribery laws and voluntary commitments applicable to its activities.
ISO/IEC 27001
ISO/IEC 27001 is the world's best-known standard for information security management systems (ISMS). It defines requirements an ISMS must meet.
The ISO/IEC 27001 standard provides companies of any size and from all sectors of activity with guidance for establishing, implementing, maintaining and continually improving an information security management system.
Conformity with ISO/IEC 27001 means that an organization or business has put in place a system to manage risks related to the security of data owned or handled by the company, and that this system respects all the best practices and principles enshrined in this International Standard.
Why is ISO/IEC 27001 important?
With cyber-crime on the rise and new threats constantly emerging, it can seem difficult or even impossible to manage cyber-risks. ISO/IEC 27001 helps organizations become risk-aware and proactively identify and address weaknesses.
ISO/IEC 27001 promotes a holistic approach to information security: vetting people, policies and technology. An information security management system implemented according to this standard is a tool for risk management, cyber-resilience and operational excellence.
Benefits
An information security management system that meets the requirements of ISO/IEC 27001 preserves the confidentiality, integrity and availability of information by applying a risk management process and gives confidence to interested parties that risks are adequately managed.
ISO 14001:2015
Environmental management systems
ISO 14001 is the internationally recognized standard for environmental management systems (EMS). It provides a framework for organizations to design, implement, and continually improve their environmental performance. By adhering to this standard, organizations can ensure they are taking proactive measures to minimize their environmental footprint, comply with relevant legal requirements, and achieve their environmental objectives. The framework encompasses various aspects, from resource usage and waste management to monitoring environmental performance and involving stakeholders in environmental commitments.
Why is ISO 14001 important?
In an age of heightened environmental consciousness and increasing global challenges such as climate change, biodiversity loss, and resource depletion, organizations have a pivotal role to play. ISO 14001 offers a structured approach for businesses to address these pressing concerns. By adopting this standard, organizations signal a commitment not only to regulatory compliance but also to ongoing environmental improvement. This proactive approach to environmental management can result in tangible benefits, such as reduced waste, energy conservation, and cost savings.
Furthermore, it enhances an organization's reputation, fosters stakeholder trust, and often meets a critical criterion for engaging in global trade and supply chains. Simply put, ISO 14001 stands as a testament to an organization's dedication to a sustainable future, blending environmental responsibility with strategic business growth.
Benefits
GMP (Good Manufacturing Practice) is the part of quality assurance that ensures consistent quality standards in the production and testing of medicinal products or active ingredients (APIs).
This is a short excerpt from the eLearning course on GMP basics
Human health is the primary concern. In everyday life, patients must feel they can rely on the high quality of a medicinal product, as they cannot check this themselves. The quality of a medicinal product is determined above all by the following factors:
The EU Guidelines to Good Manufacturing Practice require that “The holder of a Marketing Authorisation must manufacture medicinal products so as to ensure that they are fit for their intended use, comply with the requirements of the Marketing Authorisation or Clinical Trial Authorisation, as appropriate and do not place patients at risk due to inadequate safety, quality of efficacy.”
This must be proven to the competent authority, which grants approval for the medicinal product, because: without marketing authorisation, a medicinal product may not be marketed to patients. How can these requirements therefore be met? And: how can consistent quality be ensured if it is not possible to individually test each tablet that is pressed? This is the purpose of good manufacturing practice.
The principles of good manufacturing practice apply to almost all areas of a company, from research and development to production, quality control, storage and distribution. Anyone who manufactures, tests, stores or markets medicinal products or APIs on a commercial basis must therefore implement a series of defined requirements. The basic principle is that companies must manufacture medicines in such a way that they are suitable for their intended use.
The basis for GMP requirements is the CGMP (Current Good Manufacturing Practice) Guide, which the U.S. Food & Drug Administration (FDA) published in the Federal Register in 1978. With this, the authority had created the world's first legally anchored GMP regulations. These made it possible for the manufacturing processes of pharmaceutical companies to be monitored by a regulatory authority.
However, the topic also gained importance internationally: In Germany, for example, the German Medicines Act (AMG) was published in 1978 as a direct result of the thalidomide scandal. However, it did not yet contain any specific GMP requirements. It was not until 1985 that the “Pharma-Betriebsverordnung” was published. For the first time, this contained concrete GMP specifications for Germany, which formed the basis for GMP monitoring through inspections by the responsible authorities. It took another four years before the EC GMP Guidelines, which are binding for Europe, finally appeared in 1989. According to the German AMWHV §2, the guideline is now called the EU GMP Guideline and has been legally valid in Germany since 2005, which means that compliance with its specifications must be documented.
What are GMP rules?GMP rules are the requirements for quality assurance of the manufacturing processes and environment formulated by the European Commission in the principles and guidelines of Good Manufacturing Practice (GMP) for medicinal products for human use and active pharmaceutical ingredients. The EU GMP Guide describes how these rules are to be interpreted in Part I for medicinal products and in Part II for active substances, as well as in various annexes for specific product groups.
ISO/IEC 17025:2017 is an international standard specifying requirements for quality and competence in testing and calibration laboratories. The standard requires that such labs prioritise excellent quality practices and develop a reliable quality management system to establish and demonstrate their competence.
The full standard is called ISO/IEC 17025, since the certification was created by the International Organization for Standardization in conjunction with the International Electrotechnical Commission. However, many shorten this to ISO 17025 or simply 17025 certification when referring to the standard.
Ultimately, ISO 17025 is for any organization that performs testing, sampling or calibration and wants to be sure of the reliability of their results. The simplest way we can put it: if you work in a testing environment that produces measurable results, then ISO 17025 is probably applicable. This may even mean you don’t necessarily call your facility a “lab, ” but by ISO standards, you would be considered a laboratory if you are producing measurable results.
Who is ISO/IEC 17025 for?
ISO/IEC 17025 is applicable to many different testing and calibration facilities across a range of sectors. The forensics sector is an example of one area that has almost universally adopted ISO/IEC 17025 as the main indicator of quality in its labs. But laboratories in sectors as diverse as asbestos testing, acoustics, chemicals, fibre optics, food production, textiles, and even cannabis labs are certified to ISO 17025 standards.
Medical laboratories are one slight exception. Labs looking for an internationally recognised standard of quality in medical labs should look into ISO 15189 certification, as this is the standard that applies specifically to med labs. If you work in a medical lab, for example a pathology lab or in a clinical trial environment, you will find all the information you need about ISO 15189 in our dedicated knowledge hub.
ISO 17025 is of high importance for testing and calibration labs because it is globally recognized. Accreditation allows you to ensure and demonstrate the reliability of your results as well as the integrity, competence, and overall quality of your lab’s practices. It also includes demands for proficiency testing, which serves as another clear indicator of your lab’s competence. We discussed proficiency testing and its importance as part of ISO 17025 in a recent webinar.
It can be crucial to the perception of your organization as credible, trustworthy and competent to current and potential customers or business partners. That’s without even mentioning the fact that many government organisations around the world will have such accreditation as a strict prerequisite before looking to work with you.
Benefits of ISO/IEC 17025
First, Induction Stove was invented in America at the beginning of 1970, and in 1971 it was released for public use in Texas. New technology added amazing features in induction stove like temperature setting can adjust the cooking temperature as per your comfort, beautiful and practical design easy to carry, the automatic feature is the best feature as it shut down automatically it means it is safe to use. In short, an Induction stove is used for heating cooking vessels. Induction cooking allows high power, increases in temperature to be achieved, and it provides changes in heat instantly. From 01 April 2021, the Bureau of Indian Standards (BIS) has required the induction stove to be registered as per IS 302-2-6: 2009 under the Compulsory Registration Scheme from BIS, and it should conform as per IS 302-2-6: 2009.
Various typing and writing devices were invented in the whole world; the keyboard invention began with the first typing device typewriter in 1868 by Christopher Sholes. A keyboard is an input device of a computer that is used to type numbers, alphabets, and other symbols into the monitor. A keyboard has push buttons known as keys. It is considered as the input device because it sends information to the computer but does not receive any information. The keyboard is of different types like desktop or full-size keyboard, laptop keyboard, flexible keywords, handheld keywords, etc. The function of all keyboards is almost the same. The government of India has made compulsory the registration of keyboards under the Compulsory Registration Scheme. Without its registration, manufacturers are not allowed to import/export, store, distribute, or sell the keyboard in the Indian Market, and it should be manufactured as per the Indian Standard IS 13252.
A webcam is a video camera that transmits or streams an image or video in real-time to or over a computer network (Internet). A webcam is a small camera that is attached to the monitor or built into the hardware. Mostly it can be used in day to day life during video chatting includes both live audios as well as video. The main use of the webcam is for the corporate world for doing video conferencing. During the Covid situation, most of the talks, discussions, inaugurations etc., were done in video conferences. Webcams have made it possible to meet anybody, anywhere, at any time without having to travel to their location. In short, webcams are used to record moving images with the help of computers and computer networks. The Bureau of Indian Standards has made it compulsory to register the webcam under the BIS compulsory registration scheme, and it should conform as per the Indian Standard IS 616: 2017. Indian Government wants to curb the import of low-quality products. A certificate is only granted to the manufacturer if the product qualifies for the testing process.
A cash register is an electronic device which is also known as the till or Automated money handling System, which is used for registering and calculating transactions at a POINT OF SALE. The first electric cash register was invented by James Ritty and John Birch in 1879. In the initial stage, it was totally mechanical without cash receipts. It keeps all records of money in and money out also calculates taxes, generate receipt and offers basic sales tracking. It is mostly used in grocery stores and departmental stores. On 13 May 2015, the Bureau of Indian Standards (BIS) has required CASH REGISTERS to be registered as per IS 13252 (Part 1):2010 under the Compulsory Registration Scheme from the BIS Bureau of Indian Standards. According to the BIS, the cash register manufactured should conform to the Indian Standard IS 13252 (Part 1): 2010. Aleph India is here to break all the obstacles during your BIS Registration online for Cash Registers.
Automatic Teller cash dispensing Machine is also known as the ATM, which helps customers of a financial institution or bank to perform various functions like cash withdrawal, take transaction statement, fund transfer, account details, change pin, etc. It performs half of the tasks of bank officials and customers. The best thing about ATM is that it saves time and works 24*7. At any time, needy customers can withdraw money. The modern ATM is designed in such a manner that anyone can operate like an illiterate individual and specially-abled person. In short, ATMs are useful because they allow customers to execute rapid self-service activities such as deposits, cash withdrawals, bill payments, and account transfers. On 01 April 2021, the Bureau of Indian Standards (BIS) has required the Automatic Teller Cash Dispensing Machines to be registered as per IS 13252: 2010 under the Compulsory Registration Scheme from BIS. As we are all aware, day by day, cybercrime is increasing. Keeping this in consideration, BIS has certain guidelines for ATMs in order to reduce these crimes. Recently the Government of India and BIS have taken this step to maintain the quality of ATMs.
The first electronic musical system was invented at the end of the 19th century and opened a new world of sounds and compositions to the whole earth. With the advance of technology, music has come into trend, and everyone has become a music lover. On everybodys phone, we can discover a favorite music playlist. Listening to music has become the hobby of everyone. An electronic musical system is an instrument that produces sounds using electronic circuitry. Today, electronic musical systems are widely used in different styles of music. It is considered as medicine for the mind and soul, provides relaxation. On 3rd July 2013, the Bureau of Indian Standards considered all models under the category of Electronic musical System with Input Power 200W and above are required to get registered from BIS to enter the Indian Consumer Market. Electronic musical system should conform to the Indian Standards IS 616:2017. No musical system can be launched in the Indian market without the BIS Registration.
led flood light is a beamed light fixture that emits light in high intensity. led floodlights are high-intensity, wide-beamed artificial lights that are commonly used to brighten outdoor spaces. they are typically utilized on playing fields when a sporting event is being hosted in poor light circumstances. they can also be utilized for an outdoor event that needs a lot of illumination. large corporations, businesses, manufacturing plant and organizations utilize them at night to brighten their place. the best part of led flood lighting is that it does not emit the toxin elements and is totally environmental and user friendly. led flood lights are durable, strong and long lasting. the government of india with the collaboration of bis, covered led flood light under the bis registration or compulsory registration scheme as per the indian standard is 10322-5:5:2013. whether you are indian manufacture or foreign manufacturer of led flood lights, it compulsory to register it under bis registration online and obtain a compliance certificate to manufacture, import/export, sell, and store and distribute led flood light in indian market.
USB (Universal Serial Bus) Barcode Scanners use a PC computer's USB port to move or sync captured data. USB also supports hot-plugging, which allows you to plug and unplug scanners without having to restart your computer. USB ports can be found on computer desktops, laptops, and certain cell phone models. Because USB ports are directly connected to computers, scanning an item's barcode with a USB barcode scanner allows the information to be instantly transmitted to a computer database or programme. USB scanners can connect to both Android and iOS devices, making portable scanning quick and easy. The Government of India and Bureau of Indian Standards (BIS) have required BARCODE READERS to be registered as per IS 13252 (Part 1):2010 under the Compulsory Registration Scheme from BIS. BIS Registration is a must for both domestic and foreign manufacturers in order to sell products in the Indian market otherwise, it will be a punishable offence.
An automatic Data processing machine is a hardware system that automatically accumulates, processes and stores data. "An automatic data processing machine is defined as magnetic or optical readers, machines for transcribing data onto coded data medium and equipment for processing such data. Automatic data processing machines can take the form of systems made up of a variable number of individual components. Automatic Data Processing Machine automatically processes data and reduce errors. It is used in the automatic acquisition and quickly and efficiently process large amounts of information. On 3 July 2013, the Bureau of Indian Standards (BIS) has required AUTOMATIC DATA PROCESSING MACHINE to be registered as per IS 13252 (Part 1):2010 under Compulsory Registration Scheme from BIS under the Gazette of India. If you are a manufacturer of automatic data processing machines, you must register your product under a compulsory registration scheme in order to manufacture, import/export, store or sell this in the Indian market.
Television is also known as TV. The most obvious use of your television is, of course, watching it, whether it's the news, your favorite soap opera, or the latest hit drama or movie. This is the primary function of television and the purpose for its huge success. The term applies to a television set, a TV show, or the medium used to transmit television signals. Television is a popular mass-media way to advertising, entertainment, news, and sports. We depend on TV for leisure, news, education, weather forecast news, sports, culture, and even music since the beginning of music videos. As Television is an electronic device mostly used in every home, keeping this in consideration, the Government of Indian and Bureau of Indian Standards has taken a step that it is compulsory for the manufacturers to register television under Compulsory registration scheme as per IS 616: 2017. BIS have mentioned all terms and condition in the Indian Standards IS 616:2017 and must be manufactured as per the Indian Standard. It opens all the doors to the manufacturer for export/import, manufacture, sell and distribute in Indian Market.
Sealed secondary batteries are easy and safe to use. The reason behind its sealing is to prevent the spilling or loss of electrolytes when operated within the specifications. When the batteries are in use it gets discharged, then it is usually charged with electricity. Sealed Secondary Batteries are used in mobile phones, laptops, trimmers, barcode scanners, etc., which are charged with electricity. These types of batteries also include various types of chemicals, which are helpful in recharging the batteries. Rechargeable batteries are highly strong for their size and account for roughly half of all battery sales globally. In short, when a rechargeable battery comes into touch with a reverse current, it has the ability to recharge. The Government of India and BIS keeping in consideration the public health, has required it to register under the BIS Registration and should be manufactured as per the Indian Standards IS 16046:2018.
Power Inventor is a solar inverter device that converts the direct current (DC) from the solar panel into the AC alternating current. It uses natural energy solar (sun) energy to prepare the alternate current. Solar systems are made up of solar panels (or photovoltaic (PV) panels), a solar inverter (which is critical), and a rack to hold everything in place. A solar inverter or PV inverter is a type of electrical converter which converts the variable direct current (DC) output of a photovoltaic (PV) solar panel into a utility frequency alternating current (AC) that can be fed into a commercial electrical grid or used by a local, off-grid electrical network. From 30 June 2020, the Bureau of Indian Standards (BIS) has required Power Inverter to be registered as per IS 16221 (Part 2): 2015 under the Compulsory Registration Scheme from BIS. Every manufacture should register power inverters with BIS to keep them free from product compliance.
Point to sale terminal is a hardware device that is used mostly in retail stores for processing card payments. In this, debit and credit cards are used for payment purposes. The terminal's responsibilities include reading the data from a customer's credit/debit card, moving money from the customers account to the trader's, and documenting transaction details. This technology initially examines the magnetic strip on the client's credit/debit card to determine whether there is enough money to transfer to the seller. It then performs the transfer. The consumer gets the sale transaction by email or text message. In addition, the consumer can obtain a printed receipt. The best part of the point of sale terminals is that customers need not carry cash, can easily make payments using debit/credit cards.
Ghaziabad, Uttar Pradesh 
