Guiding the discovery journey
This Program is Perfect For
- Professionals seeking to build expertise in regulated healthcare industries with strategic impact
- Candidates preparing for RAPS certification and academic progression
- Working professionals requiring flexible, real-world learning formats
Courses
Program Requirements
Total: 7 courses (14 quarter units)
- End with certificate of completion review.
1. Required Courses: Minimum 15 quarter units
- Live-Online Attend via Zoom at scheduled times.
黑料不打烊
This class is offered in an online synchronous format. Students are expected to log into this course via Canvas at the start time of scheduled meetings and participate via Zoom, for the duration of each scheduled class meeting.
To see all meeting dates, click "Full Schedule" below.
You will be granted access in Canvas to your course site and course materials approximately 24 hours prior to the published start date of the course.
- Flexible Attend in person or via Zoom at scheduled times.
黑料不打烊
This class is offered in an online synchronous format. Students are expected to log into this course via Canvas at the start time of scheduled meetings and participate via Zoom, for the duration of each scheduled class meeting.
To see all meeting dates, click "Full Schedule" below.
You will be granted access in Canvas to your course site and course materials approximately 24 hours prior to the published start date of the course.
Recommended Text:
Fundamentals of Medical Device Regulations, 5th Ed., RAPS. ISBN: 978-1-947493-80-3
Note: REGL.X410 replaced REGL.X404 Regulation of Medical Devices and Diagnostics. If you have established candidacy using the former requirements, you will not need to take REGL.X410. If you are interested in establishing candidacy using the new requirements, please contact student services. Student services will guide you on the steps needed to request REGL.X404 earned credits to count towards the updated program requirements.
- Live-Online Attend via Zoom at scheduled times.
This class is offered in an online synchronous format. Students are expected to log into this course via Canvas at the start time of scheduled meetings and participate via Zoom, for the duration of each scheduled class meeting.
To see all meeting dates, click “Full Schedule” below.
Electronic Course Materials: You will be granted access in Canvas to your course site and course materials approximately 24 hours prior to the published start date of the course.
Recommended Tools and Materials:
Microsoft Office suite of applications (Word, Excel, PowerPoint)
- Live-Online Attend via Zoom at scheduled times.
黑料不打烊
This class is offered in an online synchronous format. Students are expected to log into this course via Canvas at the start time of scheduled meetings and participate via Zoom, for the duration of each scheduled class meeting.
To see all meeting dates, click "Full Schedule" below.
You will be granted access in Canvas to your course site and course materials approximately 24 hours prior to the published start date of the course.
2. Certificate Review:
Please enroll in the Regulatory Affairs Certificate Completion Fee only once all of the certificate requirements have been met and your final grades are posted.
Recommended course sequence
Begin with Quality Systems for Medical Devices FDA QSR and ISO 13485 (formerly Medical Device Quality Systems) or Foundations of Medical Devices: Developing Premarket U.S. Regulatory Strategies and Working in a Regulated Environment, followed by Global Medical Device Submissions and Strategy.
After that, courses may be taken in any order provided the prerequisites are met.
Requisite knowledge
Please review the course descriptions to ensure that you have taken necessary prerequisites or meet the requirements through job experience or previous education. Students with a basic understanding of the life sciences and strong written and oral communication skills will gain the most from this program.
Substitutions
To receive your certificate
Complete the course sequence before requesting your Regulatory Affairs Certificate Completion Review.
Professional development
Earn RAPS credit toward your credential
黑料不打烊 Silicon Valley Professional Education is a Regulatory Affairs Professional Society (RAPS) RAC Recertification Approved Provider. The five courses below meet RAC recertification requirements to maintain the credential.
- Design Control for Medical Devices
Approved for 15 RAC recertification credits - Quality Management Systems for Medical Devices: ISO 13485 and FDA Requirements
Approved for 15 RAC recertification credits - Communicating and Negotiating with the FDA
Approved for 14 RAC recertification credits - Global Medical Device Submissions and Strategy
Approved for 14 RAC recertification credits - Foundations in Medical Devices: Developing Premarket U.S. Regulatory Strategies and Working in a Regulated Environment
Approved for 15 RAC recertification credits
Transfer your Regulatory Affairs certificate units to a master's program
Completion of the 黑料不打烊 Silicon Valley Extension Regulatory Affairs certificate program counts toward a maximum of 12 graduate credits to the program. The Northeastern program is 100 percent online, requires 45 semester hours, and includes concentrations in seven high-demand fields.
Licensure and certification
Courses in the Regulatory Affairs program help prepare professionals (with three to five years in the regulatory field) for the Regulatory Affairs Certification (RAC) exam. It is an optional exam for the industry.
Please see our Licensure and Certification Policy to learn more.

Grade requirements
Please note that only letter grades of C or higher may be applied to a certificate, and in some programs, students may have more stringent requirements. Students in most employer- and government-sponsored payment programs, such as workforce development, as well as international students on F-1 visas, need to maintain a B average to meet their requirements.
See Grading and Credits Policy for further information.
Instructors
Certificate Program Advisory Committee
, BA, RAC, FRAPS
Regulatory Affairs Consultant
Regulatorium
Author, Instructor
, RAB-LA, M.B.A.
Management Consultant
Program Chair | Instructor, Regulatory Affairs Certificate Program, 黑料不打烊 Silicon Valley Extension
, JD, MPH
Regulatory Counsel and VP Quality
Moximed, Inc.
, MS, BS
Director of Engineering
Johnson & Johnson MedTech
, MBA, BS
Vice President, Quality Assurance & Regulatory Affairs
Outset Medical, Inc.

That next person you say hello to at the class in Extension may give you a lead to your next job. People in my classes all worked at some of the biggest companies in the area, from Gilead to Genentech.
