Prepare for RAPS certification. Earn credit toward recertification.
UCSC Silicon Valley Professional Education is a Regulatory Affairs Professional Society (RAPS) RAC Recertification Approved Provider.
The following courses in the Regulatory Affairs and Medical Device Quality and Design programs meet the RAC recertification requirements to maintain the credential.
Medical Device Quality and Design
- Design Control for Medical Devices
MEDD.X400
Approved for 15 RAC recertification credits
- Quality Management Systems for Medical Devices: ISO 13485 and FDA Requirements
MEDD.X407
Approved for 15 RAC recertification credits
- Validating Software for Medical Devices and Emerging Technologies
MEDD.X410
Approved for 15 RAC recertification credits - Mobile Health, SaMD, and AI/ML Devices
MEDD.X404
Approved for 9.25 RAC recertification credits
Regulatory Affairs
- Communicating and Negotiating with the FDA
REGL.X402
Approved for 14 RAC recertification credits - Global Medical Device Submissions and Strategy
REGL.X401
Approved for 14 RAC recertification credits - Foundations in Medical Devices: Developing Premarket U.S. Regulatory Strategies and Working in a Regulated Environment
REGL.X410
Approved for 15 RAC recertification credits
For more information
- Certificate Program in Regulatory Affairs
- Certificate Program in Medical Device Quality and Design
- Check with your professional organization
Every professional organization is different. Please be sure to visit the RAPS RCC website to confirm that courses still meet the requirements and to learn about any additional requirements necessary for membership, licensing, recertification, or other professional qualifications.
Licensure and Certification Policy
Certification is optional to practice in this field. Please see our Licensure and Certification Policy to learn more.