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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: Pharmaceuticals 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 regulatory profession, pharmaceuticals 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. Written for regulatory professionals in their first five years in the regulatory field, this flexible certificate program is comprehensive and customizable.
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:
Elective Courses
You also choose five courses from our entire portfolio of programs that have a P allotted to them. These courses are considered part of our Pharmaceutical certificate. You are welcome to add on additional courses outside the five “P” you select at an additional charge.
Download the Course Catalog
Registration
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.
Registration Options
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 Pharmaceuticals, 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. Learn More
RAPS and Pathway Partner to Advance Regulatory Affairs Preparedness
The Regulatory Affairs Professional Society (RAPS) and Pathway for Patient Health have partnered to advance the preparedness of regulatory affairs professionals during an unparalleled time of rapid innovation and evolving expectations. Through Pathway’s Quality Science Education Program, global thought leaders teach the why and how of product, process and systems quality across the total product lifecycle. RAPS carries this understanding of quality science into foundational and advanced regulatory affairs certificates that prepare regulatory affairs professionals for every decision they must make. Read the Press Release to learn more!