Rbm Certifications

Pimple, Pune, Maharashtra

With a comprehensive knowledge of industry, we are involved in presenting our clients a supreme range of quality services in ISO 16949 : 2009 Certification. We have a team of well experienced professionals who are able to tackle any kind of issues in the process of certification. The services on offer are executed in a timely manner. We strive to complete the services in a hassle free manner. We charge a minimal fee from our esteemed clients for our impeccable services.

What is TS 16949:2002?

• Deemed as an international quality system requirement specifically formulated for the global automotive industry.It is an ISO technical specification developed by the International Automotive Task Force, in conjunction with the members of the ISO Technical Committee-TC176.
• It details the fundamental, sector-specific, quality systems requirements that sustain continuous improvement and emphasize defect prevention while simultaneously reducing the magnitude of variation and waste in the supply chain.

TS - 16949 GOALSDevelopment of Fundamental Quality Systems that Provide for :

• Continuous Improvement.
• Defect Prevention.
• Reduction of Variation.
• Waste in the supply chain.

Coupled with Customer-specific requirement that may apply, the specification defines the fundamental quality management system requirements for those who subscribe to this document. Intended to avoid multiple certifications and to provide a common approach to Quality Management System (QMS).

Benefits of ISO/TS 16949

• Fosters improved product & process quality.
• Incorporates the best lessons learnt from the global automotive realm.
• Provides additional confidence for global sourcing.
• Ensures a global quality system approach in the supply chain for supplier/subcontractor service consistency.
• Reduces variation, waste & improves the overall efficiency in production levels.
• Eliminates the need for multiple third party registrations.
• Provides a common platform to address worldwide quality system requirements.
• Formatted to allow easy conversion to ISO9001/2000.
• Advantageous to the up gradation of existing quality systems.

Scope

• In Conjunction with ISO 9001:2008, TS defines the Quality Management System requirement for the design/ development, production and where relevant installation and servicing of automotive related products. Is applicable to production and service part organization sites where customer specified products are manufactured. Is applicable to remote locations, which however cannot obtain stand-alone certification. Applicable throughout the automotive supply chain.
• Contact us now, to get your organization ISO TS/16949 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

Making use of expertise gained in the industry over many years, we keep coming up with services meeting the exact needs of the clients. As a Service Provider, we offer yet another quality service in the form of ISO OHSAS 18001 Certification. Thanks to our specialized ISO implementation methodology, the whole process becomes less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective. Our clients can specify their requirements and we give our best to fulfill them.

What is ISO OHSAS 18001?

• OHSAS 18001 is a comprehensive Occupational Health and Safety Management System specification, designed to enable organizations to control Health & Safety risks and improve its performance. The standard is applicable to any organization that wishes to take a proactive approach to its occupational health and safety risks.
• OHSAS 18001 has been developed to be compatible with ISO 9001 and ISO 14001 to allow for easy integration. Legislative & regulatory commitment and continual improvement are two important aspects of OHSAS 18001.

The benefits of implementing a systematic and effective OH&S management system include the following :

• Reducing the number of personnel injuries through prevention and control of workplace hazards.
• Reducing the risk of major accidents.
• Ensuring a well-qualified and enthusiastic workforce by fulfillment of the increasing expectations of your     employees.
• Reducing the material loss caused by accidents and in production interruptions.
• Reducing insurance costs as well as reducing costs due to absence of employees.
• Serving the possibility for an integrated management system including quality, environment and health and safety.
• Ensuring that appropriate legislation is addressed and acted upon.
• Meeting the increasing importance of OH&S for public image.

The implementation of an Occupational Health and Safety Management System can help you to :

• Demonstrate legal compliance and reduce the risk of potential litigation.
• Reduce accidents & downtime.
• Give access to new customers and partners who require suppliers to meet tender relevant criteria.
• Reduce costs.

Contact us now, to get your organization ISO OHSAS/18001 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

We are the leading Service Provider in the industry who provides ISO 13485 Certification services. These services are imparted under strict supervision of proficient professionals making use of best tools and techniques on offer to ensure we deliver the utmost quality. Our services are widely acknowledged by our clients for prompt response and impeccable execution. We make sure the services on offer are performed in the stipulated time frame. Apart from all these features, we also make sure to go easy on our clients’ pockets by offering these services for a nominal fee.

What is ISO 13485?

• ISO 13485 is a version of the standard developed for the Medical Device Industry. It contains most of the requirements of ISO 9001 plus several additional requirements specifically for the Medical Device. It also eliminates sections of ISO 9001.ISO 13485 (and variations such as DIN EN ISO 13485) is an internationally recognized quality standard which states the requirements of the Quality Management System (QMS) for the design and manufacture of Medical Devices. While it remains a stand-alone document, ISO 13485 is based on ISO 9001 with some additional clauses as well as the removal of some requirements.
• ISO 13485is an ISO Standard, published in 2003. The ISO 13485 was designed for organizations that provide medical devices or related services. It provides the requirements for a comprehensive management system for the design and manufacture of medical devices.ISO 13485 is generally harmonized with the ISO 9001 standard, though it is a stand-alone document. ISO 13485 removes ISO9001’s emphasis on continual improvement and customer satisfaction though it has been developed based on ISO 9001. It lays emphasis on meeting regulatory as well as customer requirements, risk management and maintaining effective processes, namely the processes specific to the safe design, manufacture and distribution of medical devices.

Benefits of ISO 13485The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. To ensure this, it includes some particular requirements for medical devices and excludes some of the requirements of ISO 9001 that are not appropriate as regulatory requirements.Organizations whose quality management systems conform to this International Standard cannot claim conformity to ISO 9001 unless their quality management systems conform to all the requirements of ISO 9001 because certain points have been excluded in ISP 13485.

Benefits of ISO 13485

• Once you get ISO 13485 certification, it will help your organization do business in this highly regulated sector. It will demonstrate that your organization is committed to quality, customers, and is willing to work towards improving efficiency.ISO 13485 promotes harmonization of regulatory requirements for manufacturers of medical devices on an international scale.
• Contact us now, to get your organization ISO 13485 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

Backed by the well trained staff, we as a Service Provider offer ISO 14001 : 2004 Certification services. Renowned for its effective and systematic execution, the services on offer are provided by a team of skilled experts. At our end, we make sure the quality of our services is never compromised. The timely execution of services makes us an instant hit among the clients. These quality services are made available by us for a cost effective fee for our valued clients. Get in touch to avail our services.

What is ISO 14001:2004?

• Organizations of all kinds are increasingly concerned with achieving and demonstrating sound environmental performance by controlling the impacts of their activities, products and services on the environment, consistent with their environmental policy and objectives.
• This International Standard specifies requirements for an environmental management system to enable an organization to develop and implement a policy and objectives which take into account legal requirements and information about significant environmental aspects. It is intended to apply to all types and sizes of organization and to accommodate diverse geographical, cultural and social conditions. The overall aim of this International Standard is to support environmental protection and prevention of pollution in balance with socio-economic needs.

This International Standard requires an organization to

• Establish an appropriate environmental policy.
• Identify the environmental aspects arising from the organizations past, existing or planned activities, products and services, in order to determine the environmental impacts of significance.
• Identify applicable legal requirements and other requirements, to which the organization subscribes.
• Identify priorities and set appropriate environmental objectives and targets.
• Establish a structure and a program(s) to implement the policy and achieve objectives and meet targets.
• Facilitate planning, control, monitoring, preventive and corrective actions, auditing and review activities to ensure both that the policy is complied with and that the environmental management system remains appropriate.
• Be capable of adapting to changing circumstances.

Some of the benefits experienced by companies implementing ISO 14001 include :

• Process improvement.
• Environmental cost reduction.
• Better relationships with regulators.
• Better relationships with insurers, investors, and financial markets.
• Product improvement.
• Marketing advantages.
• Better control of liabilities.
• Reduced regulatory burden.
• Protection of company image and name.
• Demonstration of responsible management.

ISO 14001 is a process-oriented standard; it implies a commitment to continuous improvement.Contact us now, to get your organization ISO 14001 : 2004 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

Sitting in the upper echelons among leading players of the industry, we, as a Service Provider, strive to meet the expectation of our clients to the fullest. Aligned with our reputation, we present equal excellence in ISO 27001 : 2005 Certification. We strive to deliver our services well within the scheduled time frame. It makes our services admired by our clients all over the world. On the back of qualified and committed staff, we are able to provide our services with perfection.

What is ISO 27001:2005?

• ISO 27001:2005 certification (Information Security Management System). is the standard, which specifies requirements for implementation, establishment, operation, monitoring, research, maintenance and improvement of documented Information Security Management Systems (ISMS). It specifies requirements for establishment of a safety control, adapted according to needs of an organization. The organization declares the assurance of information security management system requirements by certification according to BS 7799-2 / ISO 27001:2005 certification.
• ISO 27001 certification specifies the Plan-Do-Check-Act (PDCA) model for continual quality improvement. The PDCA cycle helps "the organization to know how far and how well it has progressed" and "influences the time and cost estimates to achieve compliance." ISMS as "a systematic approach to managing sensitive company information so that it remains secure. ISMS encompasses people, processes, and IT systems."
• Information security is achieved by applying a suitable set of controls (policies, processes, procedures, organizational structures, and software and hardware functions).  ISO 27001 certification is suited to any organization that manages assets - data, people, software and intellectual property. This includes government departments (or their critical suppliers such as mailing houses, or data warehouses), energy providers and utilities, banks, insurance companies and corporate across all sectors of the economy.

Some of the benefits experienced by companies implementing ISO 27001:2005include :

• A valuable framework for resolving security issues.
• Enhancement of client confidence & perception of your organization.
• Enhancement of business partners confidence & perception of your organization.
• Provides confidence that you have managed risk in your own security implementation.
• Enhancement of security awareness within an organization.
• Assists in the development of best practice.
• Can often be a deciding differentiator between competing organizations.

Contact us now, to get your organization ISO 27001 : 2005 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

Keeping abreast with the latest demands in the industry, we enable ourselves to cater to the clients’ needs to perfection. As a leading Service Provider, we offer ISO 9001 : 2008 Certification services to our clients. We are admired in the industry for our promptness and commitment. Get in touch to avail it in an efficient and effective manner. Thanks to our specialized ISO implementation methodology, the whole process becomes less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

What is ISO 9001:2008?ISO 9001:2008 is the revised edition ISO 9001 : 2000 &latest version of a quality management standard which has been in existence for many years and which has been applied by more than 500, 000 organizations world-wide in 145 countries. It is a generic standard applicable to any type of organization / institute irrespective of size / nature of work. It provides an organization with a set of principles that ensure focused, informed, scientific and proven approach to the management of your business activities to consistently achieve customer satisfaction and continually improve operational effectiveness.

It specifies minimum requirements for a quality management system where an organization needs to :

• Demonstrate its ability to provide consistently a product that meets customer and applicable regulatory requirements.
• Address customer satisfaction through the effective application of the system, developing processes for continual - improvement and the prevention of errors and mistakes.

It is based on following eight management Principles :

• Customer Focus
• Leadership
• Involvement of People
• Process Approach
• System approach to Management
• Continual Improvement
• Factual approach to decision making
• Mutually Beneficial supplier Relationships

Perceived benefits/advantages of ISO 9001:2008 certification
Improvement in "bottom line" profit through

• Consistent control of key processes.
• Reduce Cost in all area as result of Effective Management.
• Better efficiency, Reduces Waste & Continual improvement.
• Improves Business Performance.
• The Effective Management of Risk.
• Encourages internal communication and raises morale
• IncreasesCustomer Satisfaction.
• Promotion, Greater Marketing Appeal and Improved Public Relations.
• World-Wide Recognition for Good Working Practices& Removes Barriers to trade.
• Meeting the requirements for inclusion on some tender lists.

Leveraging on the capability of our talented staff, we are immersed in offering ISO HACCP 22000 Certification services. Clients may specify their requirements and provision and our team executes the services in compliance of the same. Making use of modern methods, we are able to execute the services well within the specified time frame. Our services are found as an enjoyable experience by our clients. Our success rate is close to 100% which makes us admired among our valued clients.

What is ISO HACCP/ 22000?HACCP is a management system in which food safety is addressed through the analysis and control of biological, chemical, and physical hazards from raw material production, procurement and handling, to manufacturing, distribution and consumption of the finished product. Preventing problems from occurring is the paramount goal underlying any HACCP system. Benefits, in addition to enhanced assurance of food safety, are better use of resources and timely response to problems.

HACCP PRINCIPLESHACCP is a systematic approach to the identification, evaluation, and control of food safety hazards based on the following seven principles :

• Principle 1 : Conduct a hazard analysis.
• Principle 2 : Determine the critical control points (CCPs).
• Principle 3 : Establish critical limits.
• Principle 4 : Establish monitoring procedures.
• Principle 5 : Establish corrective actions.
• Principle 6 : Establish verification procedures.
• Principle 7: Establish record-keeping and documentation procedures.

HACCP is designed for use in all segments of the food industry from growing, harvesting, processing, manufacturing, distributing, and merchandising to preparing food for consumption. Prerequisite programs such as current Good Manufacturing Practices (cGMPs) are an essential foundation for the development and implementation of successful HACCP plans. The principles of HACCP have been universally accepted by government agencies, trade associations and the food industry around the world.
Objectives of Implementing a Food Safety and Food Quality Program :-By implementing a food safety and food quality program, we can eliminate costs that result from poor quality and unsafe food products. Poor quality, for example, can be spotted as defective product, wastage, and product returns.

Besides, there are other costs associated with poor quality control such as :

• Reduction in Shelf Life.
• Loss of Customers.
• Reduction in Repeat Sales.
• Production Line Downtime.
• Excess Inventory.
• Product Liability.

Contact us now, to get your organization ISO/HACCP 22000 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

We, being a distinguished name in the market, indulge ourselves in offering GMP Certification services. We meet the customized requirements of the clients being a devoted Service Provider. Our dependable services are applauded worldwide by our clients. Get in touch to avail it in an efficient and effective manner. Thanks to our specialized ISO implementation methodology, the whole process becomes less time consuming, easy to understand and implement, result oriented, time bound and cost effective. The services on offer are available for a reasonable fee.

What is GMP Certification?

• Good manufacturing practice" or "GMP" is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidelines that outline the aspects of production and testing that can impact the quality of a product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation.
• GMP guidelines are not prescriptive instructions on how to manufacture products. They are a series of general principles that must be observed during manufacturing. When a company is setting up its quality program and manufacturing process, there may be many ways it can fulfill GMP requirements. It is the company's responsibility to determine the most effective and efficient quality process.

Principles of GMP Standards :

• Manufacturing processes are clearly defined and controlled. All critical processes are validated to ensure consistency and compliance with specifications.
• Manufacturing processes are controlled, and any changes to the process are evaluated. Changes that have an impact on the quality of the drug are validated as necessary.
• Instructions and procedures are written in clear and unambiguous language. (Good Documentation Practices)
• Operators are trained to carry out and document procedures.
• Records are made, manually or by instruments, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the drug was as expected. Deviations are investigated and documented.
• Records of manufacture (including distribution) that enable the complete history of a batch to be traced are retained in a comprehensible and accessible form.
• The distribution of the drugs minimizes any risk to their quality.
• A system is available for recalling any batch of drug from sale or supply.
• Complaints about marketed drugs are examined, the causes of quality defects are investigated, and appropriate measures are taken with respect to the defective drugs and to prevent recurrence.

Contact us now, to get your organization GMP certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

Backed by the well trained staff, we as Service Provider offer our clients ISI Mark Certification services. Renowned for its effective and systematic execution, the services on offer are provided by a team of skilled professionals. At our end, we make sure the quality of our services is never compromised. The timely execution of services makes us an instant hit among the clients. These quality services are made available by us for a cost effective fee for our valued clients. Get in touch to avail our services.

What is ISI Marking?

• ISI stands for the Indian Standards Institute, a body set up when India gained Independence to create standards needed for orderly commercial growth and maintaining quality in industrial production. In 1986 the government recognized the need for strengthening this National Standards Body due to fast changing socio-economic scenario and according it a statutory status. Thus came the Bureau of Indian Standards Act 1986 and on 1 April 1987, newly formed BIS took over staff assets, liabilities and functions of erstwhile ISI. Through this change over, the Government envisaged building of the climate of quality culture and consciousness and greater participation of consumers in formulation and implementation of National Standards
• BIS is authorised by a legislation of 1986 to offer product certification. This certification programme is basically voluntary. Any manufacturer who feels confident enough that his product has the ability to meet the BIS standard can apply for product certification.
• We offer one of the best services as ISI consultants to all the companies irrespective of their sizes and nature. We provide with ISI certification services in which we help you achieve ISI certificate by improving you management system and thereby your quality standards. By this you not only get an ISI certificate but your company benefits on a whole as it starts working in a better manner. By our efforts, we have also gained the position of one of the renowned ISI certification consultants in India.
• The Product Certification Scheme of BIS aims at providing Third Party Guarantee of quality, safety and reliability of products to the ultimate customer. Presence of ISI certification mark known as Standard Mark on a product is an assurance of conformity to the specifications. The conformity is ensured by regular surveillance of the licensee's performance by surprise inspections and testing of samples, drawn both from the market and factory.

Contact us now, to get your product ISI certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

We have gained expertise by offering a superior range of ISO 20000 Certification services. We hire a team of skilled professions who are well versed in delivering these services. Our high success rate translates into high satisfaction among our clients. We make our services available all day round every day. We carry out our services without any hassles. The timely execution of services makes us popular among our esteemed clients. For providing our services, we make use of specialized methodology.

Additional Information :ISO/IEC 20000 is the first international standard for IT service management. It was developed in 2005, by ISO/IEC JTC1 SC7 and revised in 2011.[1] It is based on and intended to supersede the earlier BS 15000 that was developed by BSI Group.

It consists of two distinct parts :

• The Specification : ISO20000-1 defines the requirements for a service provider to deliver managed services.
• The Code of Practice : ISO20000-2 describes detailed best practices for the processes defined within ISO 20000-

Overall, these standards specify five key group service management processes: Service Delivery, Relationship, Resolution, Control and Release.Formally: ISO/IEC 20000-1 ('part 1') "promotes the adoption of an integrated process approach to effectively deliver managed services to meet the business and customer requirements". It comprises ten sections :

• Scope
• Terms and definitions
• Planning and implementing service management
• Requirements for a management system
• Planning and implementing new or changed services
• Service delivery processes
• Relationship processes
• Control processes
• Resolution processes
• Release process.

Contact us now, to get your organization ISO/IEC 20000 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

We, being a distinguished name in the market, indulge ourselves in offering ISO 50001 : 2011 Certification services. We meet the customized requirements of the clients being a devoted Service Provider. Contact us now get your hand on it in an efficient and effective manner. The whole process becomes less time consuming, fast, easy to understand and implement, result oriented and cost effective owing to our specialized ISO implementation methodology. We make sure the services on offer are performed in the stipulated time frame.

What is ISO 50001 : 2011?

• ISO 50001:2011 is a first standard for energy management system published by ISO on June 2011. ISO 50001 has provides structured framework for organizations to manage and control energy that it can increase energy efficiency, reduce costs and improve energy performance. ISO 50001 is intended to help business make better use of your energy consumption or energy performance through a systematic approach.
• The standard is compatible with other management system especially ISO 14001 (Environmental Management System) and ISO 9001 (Quality Management System). ISO 50001 is based on the Plan-Do-Check-Act (PDCA) cycle and it integrates to works both the technical and managerial activities.

Key Features of Energy Management System :

• The standard has defines your energy policy, objective and targets that relate to use of energy.
• Continual improvement in the energy performance
• Its Create transparency and facilitate communication on the management of energy resources and promotion of energy.
• Periodically review the energy use, consumption and efficiency.
• Prioritization of issues affecting energy use and efficiency
• It reduces the costs and Green House Gas (GHG) emissions.
• Formalizing control systems and monitoring processes has works based on PDCA cycle.
• Evaluation of compliance with legal and other requirements.

Benefits of Achieving ISO 50001 Standard :

• ISO 50001 standards have clearly specify the requirements of energy management of organization.
• Its help to frame the opportunities for to improve the energy management.
• Continually improve energy management.
• Reduces the carbon emissions and other environmental collision.
• Its create loyalty to business that it can increase the customer and shareholders.

Contact us now, to get your organization ISO 50001 : 2011 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.

ISO 31000:2009 provides principles and generic guidelines on risk management. ISO 31000:2009 can be used by any public, private or community enterprise, association, group or individual. Therefore, ISO 31000:2009 is not specific to any industry or sector. It 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.
ISO 31000:2009 can be applied to any type of risk, whatever its nature, whether having positive or negative consequences. Although ISO 31000:2009 provides generic guidelines, it 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.
Contact us now, to get your organization ISO 31000 : 2009 certified in the most effective and efficient manner while realizing the true benefits of the certification using our specialized ISO implementation methodology that is less time consuming, fast, easy to understand and implement, result oriented, time bound and cost effective.