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Medical Device and Diagnostic Industry (MD+DI) is the primary resource for manufacturers of medical devices and in vitro diagnostic products. Its mission is to help medtech industry professionals develop, design, and manufacture products that comply with complex and demanding regulations and evolving market requirements. For nearly 40 years, MD+DI's editorial quality and reliability have won it an unparalleled degree of trust from the industry. Some of the best and brightest experts in medtech contribute to MD+DI, and many of their articles have become standards of reference for the medical device industry.

Housed on the MD+DI site, Qmed is the world’s only directory of pre-qualified suppliers and service providers to the medical device and diagnostics industry. Since 2010, Qmed’s powerful search tool and online directory have enabled medtech manufacturers to find relevant partners who can help fill the gaps in their current capabilities. To be considered for inclusion in the Qmed directory, companies must show qualification through some of the following criteria:

  • ISO 9001 certification
  • ISO 13485 certification
  • CGMP compliance
  • FDA registration
  • Demonstrated experience with clients in the medical device or in vitro diagnostics space

Along with our associated MD&M and BIOMEDevice live events, MD+DI and Qmed provide the information and connections medtech professionals need to design, develop, and manufacture products that save and improve lives.

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