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2020 - Risk Management in Medical Devices Industry

Date2020-06-04 - 2020-06-05

Deadline2020-05-25

VenueBoston, MA, USA - United States USA - United States

KeywordsISO 14971 workshop; ISO 13485; Quality system integration

Websitehttps://www.complianceonline.com/medical...

Topics/Call fo Papers

By attending this seminar you will learn the main elements of ISO 14971, ISO 13485, IEC62304, IEC62366-1/-2, risk management life cycle steps and benefits, and FDA software reviewers' guidance.

Other CFPs

  1. Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
  2. Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
  3. Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
  4. Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
  5. International Conference on Education, Business and Social Science(ICEBSS-2020) SCOPUS, SSRN indexed

Last modified: 2020-02-14 23:14:37