Getting timely FDA approval so products can get to market quickly, is the function of a regulatory affairs professional. Our Specialized Studies Program is designed to give professionals a core competency in managing the regulatory process, FDA approval process, and an understanding of the product life-cycle.
Participants who complete the program will satisfy the Level I and II core competencies described in the RAPS Regulatory Affairs Professional Framework.
Specialized Studies Award Requirements
Candidates must possess a fundamental understanding of FDA regulations through Regulatory Requirements for Medical Devices, EECS X445.2, or Regulatory Requirements for Pharmaceutical Products, EECS X445.26; OR possess equivalent experience or education.
NOTE: Candidates choose either Regulatory Requirements for Medical Devices OR Regulatory Requirements for Pharmaceutical Products. Candidates that choose to take both courses may count one as an required course.
The Specialized Studies certificate is provided upon successful completion of three required courses totaling 9 units, with a grade point average of “B” or better. To receive your certificate, submit a Request for Certificate after completing all program requirements. Students not pursuing a specialized studies award are welcome to take as many individual courses as they wish.
Note: Six credit units may be counted toward the Medical Product Development or Clinical Trials: Medical Device and Drug Development Certificate Program.
Regulatory Affairs Management
Regulatory Affairs: An Opportunity to Excel in Biotechnology
- Prepare for a job transition into the life science industry
- Further your career as a regulatory affairs professional
- Earn credits to qualify for RAC recertification
- UC Irvine Extension is a RAPS registered provider for professional development
- Organize your company’s clinical and regulatory strategies
- Establish an educational pathway for advanced education in FDA regulations, compliance, and policy
Who Should Enroll
This program is designed for individuals who ensure regulatory compliance and prepare submissions for their organization’s products for FDA approval. Job functions include addressing laws, regulations, policies and guidelines for regulated health products, medical devices, pharmaceuticals, biologics, and biotechnology.
On-site Training Available
Through Corporate Training, we can deliver this program or customize one that fits
your organization's specific needs. Visit Corporate Training
or call (949) 824-1847 for information.