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RoHS is the acronym for Restriction of Hazardous Substances. RoHS, also known as Directive 2002/95/EC, originated in the European Union and restricts the use of specific hazardous materials found in electrical and electronic products. All applicable products in the EU market after July 1, 2006 must pass RoHS compliance.
RoHS applies to these products in the EU whether made within the EU or imported. Certain exemptions apply, and these are updated on occasion by the EU. RoHS only applies to 10 categories of electrical products sold or produced in Europe and China. RoHS takes effect on July 1, 2006. The directive applies to all
ISO 9001:2015 (QMS)9001:2015 certification has been in place for over a decade now and is used by both customers and companies as a method of controlling their quality.The Standard provides a framework to manage your business and ensure a philosophy of continual improvement in all aspects of your business.Involves Top management in the improvement of the Quality management System Facilitates the organization to become a customer-focused organization.
Ensures sustained customer satisfaction by producing, delivering services and providing support functions that meet customer's needs and expectations. Increases the effectiveness and efficiency of the organization through continual improvement in systems and products /services quality.Customer focusLeadershipInvolvement of peopleProcess approachSystem approach to managementContinual improvementFactual approach to decision makingMutually beneficial supplier relationshipsImproved outcome of processProfessional imageIncreased customer confidenceBetter marketabilityClarity of responsibility and authorityBetter and defined systemConsistent Quality
ISO-14001:2004 (EMS)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
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
Advantages of ISO 14001:2004
OHSAS 18001:2007 (OHSAS)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.
Policy and commitmentHazard identification, risk assessment & risk controls
Legal requirements Objectives & Programs Organization & personnel Training, Communication & Consultation
Documentation & recordsOperational ControlsEmergency ReadinessMeasurement & monitoringAccident & incident investigation, corrective & preventive action
ISO 22000:2005 (FSMS)This International Standard ISO 22000 specifies requirements for a food safety management system where an organization in the food chain needs to demonstrate its ability to control food safety hazards in order to ensure that food is safe at the time of human consumption.
This International Standard ISO 22000 specifies requirements to enable an organization
To plan, implement, operate, maintain and update a food safety management system aimed at providing products that, according to their intended use, are safe for the consumer
To demonstrate compliance with applicable statutory and regulatory food safety requirements
To evaluate and assess customer requirements and demonstrate conformity with those mutually agreed customer requirements that relate to food safety, in order to enhance customer satisfaction
To effectively communicate food safety issues to their suppliers, customers and relevant interested parties in the food chain
To ensure that the organization conforms to its stated food safety policy
To demonstrate such conformity to relevant interested parties and To seek certification or registration of its food safety management system by an external organization, or make a self-assessment or self-declaration of conformity to this International Standard.
Good Manufacturing Practice (GMP)is a part of quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, food, pharmaceutical products and medical devices. GMP Certification confirms the products identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given.
Benefits
ISO / TS 16949:2009(This standard is Applicable in Automobile Industries) Benefits of ISO/TS 16949
CE MARKCE Marking is a specific procedure that is to be ensured for a wide variety of products and one, which manufacturers located in the EU or importers of goods into the EU must complete. The CE mark is affixed to the product as the final stage of this procedure and is effectively a statement from the manufacturer (or importer) that the process has been successfully completed and that the product meets the essential requirements of the relevant CE marking Directives
The CE Marking Is Required Only for the Following Types of Products:Toys, Machinery, Electrical equipment, Electronic equipment, Personal protective equipment, Pressure equipment, Medical devices, Active implantable medical devices, In vitro diagnostic medical devices, Radio and Telecommunications terminal equipment, Simple pressure vessels, Gas appliances, Lifts, Recreational craft, Equipment and protective systems for use in explosive atmospheres, Non-automatic weighing instruments, Cableways, Construction products, Explosives for civil use, New hot water boilers, Measuring Equipment.
ISO 13485 ( Medical device)ISO 13485 is an international standard that specifies requirements for a quality management system that can be used by an organization for the design and development, production, installation, and servicing of medical devices. This standard can also be used by international and external parties, including certification bodies, for assessment of the organization's ability to meet customer and regulatory requirements. The quality management system requirements specified in the ISO 13485:2003 standard complements technical requirements for products. The primary purpose of the ISO 13485:2003 standard is to facilitate harmonized medical device regulatory requirements for quality systems. All requirements of the ISO 13485:2003 standard are specific to organizations providing medical devices, regardless of the type or size
ISO -27001-2005 (Information security management system)The final version of ISO 27001 was published in October 2005 to a great fanfare. It should be noted, however, that this is in fact only the first of a series of standards to support information security. Having stated this, it may well be the most important, at least from a 'top down' perspective, as it defines the information security management system
Kosher foods are those that conform to the rules of Jewish religion. These rules form the main aspect of kashrut, Jewish dietary laws.
Reasons for food being non-kosher include the presence of ingredients derived from non-kosher animals or from kosher animals that were not properly slaughtered, a mixture of meat and milk, wine or grape juice (or their derivatives) produced without supervision, the use of produce from Israel that has not been tithed or even the use of cooking utensils and machinery which had previously been used for non-kosher food.For Kosher Certification, Kosher Consultancy, Kosher Documentation, please contact us for further information.
