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This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
The Regulatory Affairs Certificate: Medical Devices provides a cost-effective, convenient option that will equip you or your organizational team with the tools and knowledge needed to progress as a regulatory professional and stay ahead of the competition.
Whether you are new to the profession, medical devices industry, transitioning from a related discipline or simply need to refresh your knowledge, this comprehensive and flexible resource will meet the learning needs of you as an individual or your entire team.
This certificate is achieved by completing four (4) core and five (5) elective courses. After successfully completing all nine courses, you will receive a certificate recognizing your achievement.
You will have twelve months (12) to complete all nine (9) courses of the program.
The following four courses are required as part of the program requirements:
You also choose five courses from our entire portfolio of programs that have a M allotted to them. These courses are considered part of our Medical Device certificate. You are welcome to add on additional courses outside the five “M” you select at an additional charge.
Download the Course Catalog
Note: If you have already registered for a RAPS Online University course that is included as part of this certificate program, you may be able to apply it toward the program requirements and registration fee. Contact us to see if your course(s) qualifies.