The Regulatory Affairs Certificate: Medical Devices provides a cost-effective, convenient option that will equip you with the tools and knowledge needed to progress as a regulatory professional and stay ahead of the competition. Written for regulatory professionals in their first five years in the regulatory field, this certificate program is comprehensive and flexible to meet your learning needs.
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 six months
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 the M assigned to them. These courses are considered part of our Medical Device certificate. You are welcome to add on additional courses outside the five “M” courses you select at an additional charge.
More questions about the certificate program? Check out the certificate FAQs
Dual Certificate Upgrade
If you have already successfully completed a Regulatory Affairs Certificate in Medical Devices, you can complete the two remaining core courses of the Dual Certificate
, not taken as part of your original Certificate program, and three additional electives to receive recognition of satisfactory achievement of the Dual Certificate.