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ISO 9000

The ISO 9000 family of quality management systems QMS is a set of standards that helps organizations ensure they meet customer and other stakeholder needs within statutory and regulatory requirements related to a product or service ISO 9000 deals with the fundamentals of QMS including the seven quality management principles that underlie the family of standards

Get Credentialed

Experience must be completed at a laboratory accredited/approved by JCI CAP ISO 15189 or authorized by a governing regulatory association or Ministry Countries without a prevalent system of accreditation must have laboratories approved by an International Advisory Board appointed by the ASCP Board of Certification

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ISO 13485

ISO 13485 Medical devices Quality management systems Requirements for regulatory purposes is an International Organization for Standardization ISO standard published for the first time in 1996 it represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices This standard supersedes earlier documents such as EN 46001 1993

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Company Profile

Certvalue A division of BLIP SNIP Consulting PVT LTD is a global leader in consulting training and certification as a one stop solution for ISO CE marking HACCP GMP HALAL ROHS BIFMA and many more delivering high quality services with complete focus on Customer satisfaction As a trusted partner we go beyond certification and educate

ISO 9001

ISO 9001 is one of the standards within the range of ISO 9000 standards Meeting the requirements of ISO 9001 will provide quality management systems that will be of real benefit to your organisation to help manage your business effectively and put in place best practice methodology ISO 9001 certification will give your organisation the

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CE Marking

Step 2 Identify the conformity assessment procedure that must be taken This could be self declaration involve testing inspection or quality system assessment from a Notified Body or a combination of these The conformity assessment procedure will differ depending on your product and the Directive in respect of which you will be CE Marking

Bureau Veritas Certification

Certification is not just an event It s a process of audits and monitoring that verify compliance Bureau Veritas aim is to make that process as simple and transparent as possible The certification process typically comprises seven distinct steps each validated by a deliverable from Bureau Veritas It is generally a three year program

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What is the relationship between FDA s Quality System

many of their customers want them to have ISO 9001 certification most medical device manufacturers choose to use ISO 13485 or EN 46001 to obtain a CE mark These standards which are currently


ISO 13485 is designed to be used by organizations involved in the design production installation and servicing of medical devices and related services It can also be used by internal and external parties such as certification bodies to help them with their auditing processes

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Scope CASCO membership is open to interested member bodies as participating P or observer O members and to interested correspondent members as observer O members To study means of assessing the conformity of products processes services and management systems to appropriate standards or other technical specifications

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The International Accreditation Forum IAF is a worldwide association of accreditation bodies and other bodies interested in conformity assessment in the fields of management systems products processes services personnel validation and verification and other similar programs of conformity assessment

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ISO 9001 sets out the criteria for a quality management system and is the only standard in the family that can be certified to although this is not a requirement It can be used by any organization large or small regardless of its field of activity In fact there are over one million companies and

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Conformity Assessment

We have been working with Szutest since 2015 CE marking conformity assessment and certification services provided by Szutest team especially solution oriented approaches which have made a significant contribution to our fruitful cooperation exceeded our highest expectations We believe that in the future Szutest will continue to grow as well

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CE marking

On commercial products the letters CE as the logo mean that the manufacturer or importer affirms the good s conformity with European health safety and environmental protection standards 58 It is not a quality indicator or a certification mark The CE marking is required for goods sold in the European Economic Area EEA but is also found on products sold elsewhere that have been

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