Regulatory Affairs Professional Credit | UCSC Silicon Valley Extension

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.