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

Medical discovery and commercialization

Students in the Regulatory Affairs certificate program learn to navigate the intricate regulatory landscape of medical devices. They embark on a journey of discovery that emphasizes patient safety, ethics, and compliance, gaining a thorough understanding of regulatory intelligence, federal regulations, and global regulatory requirements. Students learn:

  • Best practices for interacting and negotiating with the FDA.
  • Regulatory submission writing.
  • Risk management strategies in the product lifecycle.
  • A foundation for the Regulatory Affairs Certification (RAC) exam (administered by the Regulatory Affairs Professionals Society).

Join our industry-wide network of instructors and classmates who share your passion for developing regulatory strategies for the global marketplace.

Regulatory Affairs certificate program learning objectives

  • Develop a global regulatory strategy for medical devices, drugs, and biologics.
  • Identify how regulatory affairs and quality compliance professionals contribute to an organization’s bottom line by keeping up with global regulatory requirements.
  • Understand and apply good manufacturing practices (GxPS/cGMPS) and quality system regulation for drugs, biologics, and medical devices to help an organization achieve sustainable compliance.
  • Apply risk management principles when conducting post-market surveillance activities such as recalls and market corrections.
  • Communicate in writing and verbally with corporate executives.
  • Negotiate with regulatory agencies such as the FDA.
  • Demonstrate knowledge of the design and development life cycle approach for drugs and biologics medical devices and have knowledge on how to compile a design history.

Prepare for RAPS certification. Earn credit toward recertification.

黑料不打烊 Silicon Valley Professional Education is a Regulatory Affairs Professional Society (RAPS) RAC Recertification Approved Provider. See the Professional Development section below for courses that meet RAC recertification requirements to maintain the credential.

Courses

Program Requirements

Total: 7 courses (14 quarter units)

  • End with certificate of completion review.

1. Required Courses: Minimum 15 quarter units

REGL.X402
$750
  • Live-Online Attend via Zoom at scheduled times.
Schedule
Date
Start Time
End Time
Meeting Type
Location
Tue, 02-24-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 02-24-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-03-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-03-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-10-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-10-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-17-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-17-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-24-2026
6:00pm
9:00pm
Live-Online
REMOTE
Tue, 03-24-2026
6:00pm
9:00pm
Live-Online
REMOTE
 

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.

Winter
MEDD.X400
$795 (Estimated Cost)
Currently no classes scheduled. Would you like to be notified when a class is available?
Fall Live-Online
REGL.X410
$795
  • Flexible Attend in person or via Zoom at scheduled times.
Schedule
Date
Start Time
End Time
Meeting Type
Location
Thu, 02-26-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 02-26-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-05-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-05-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-12-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-12-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-19-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-19-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-26-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 03-26-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 04-02-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 04-02-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 04-09-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
Thu, 04-09-2026
6:00pm
9:00pm
Flexible
SANTA CLARA / REMOTE
 

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.

Winter
REGL.X401
$750
  • Live-Online Attend via Zoom at scheduled times.
Schedule
Date
Start Time
End Time
Meeting Type
Location
Sat, 11-22-2025
8:30am
1:30pm
Live-Online
REMOTE
Sat, 11-22-2025
8:30am
1:30pm
Live-Online
REMOTE
Sat, 12-06-2025
8:30am
1:30pm
Live-Online
REMOTE
Sat, 12-06-2025
8:30am
1:30pm
Live-Online
REMOTE
Sat, 12-13-2025
8:30am
1:30pm
Live-Online
REMOTE
Sat, 12-13-2025
8:30am
1:30pm
Live-Online
REMOTE
 

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)

Fall Live-Online
REGL.X400
$875 (Estimated Cost)
Currently no classes scheduled. Would you like to be notified when a class is available?
Currently no classes scheduled. Would you like to be notified when a class is available?
Currently no classes scheduled. Would you like to be notified when a class is available?
REGL.X405
$860
  • Live-Online Attend via Zoom at scheduled times.
Schedule
Date
Start Time
End Time
Meeting Type
Location
Wed, 02-11-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 02-11-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 02-18-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 02-18-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 02-25-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 02-25-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-04-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-04-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-11-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-11-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-18-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-18-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-25-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 03-25-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 04-01-2026
6:00pm
9:00pm
Live-Online
REMOTE
Wed, 04-01-2026
6:00pm
9:00pm
Live-Online
REMOTE
 

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.

Winter

2. Certificate Review:

O-CE0364
$95 (Estimated Cost)
Schedule
Date
Start Time
End Time
Meeting Type
Location
 

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.

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.

Program Chair

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.

Fred Bauzon

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.

Fred Bauzon,
Field Application Scientist and Molecular Biologist
Demo