The medical device industry faces specific challenges when bringing their products to the global market.
Medical devices are subject to strict and complex global regulations. Since medical devices are subject to risk, every organization in the supply chain is required to maintain an adequate quality management system. Intertek’s medical device auditing and certification services will provide you with our third-party systems verification carried out by our industry experts.

Intertek is a leading Total Quality Assurance provider of assurance, inspection, testing, certification services for the medical industry. Our unique combination of in-depth knowledge and global presence has brought confidence and peace of mind to thousands of organizations all over the world. 

Intertek’s medical devices auditing and certification services include:

ISO-13485
ISO 13485
MDSAP
Medical Device Single Audit Program (MDSAP)
MDD
Medical Device Directive (MDD)
ICMED
ICMED - Indian Certification of Medical Devices
ISO-22716
ISO 22716:2007 - Cosmetics GMP
MDR
Medical Device Regulation (MDR)
 
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ISO/IEC 27001 – Information Security Management
ISO 45001 - Occupational Health and Safety Management
ISO 22301 – Business Continuity Management
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Intertek offers a unique portfolio of assurance, testing, inspection, and certification solutions for the Medical Device and Healthcare industry.
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