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BILL KURANI, M.S.R.A., M.S.E.E., is head and director of regulatory affairs and quality assurance at a Silicon Valley-based global genomics company. He has over 20 years of experience in regulatory affairs and quality assurance and has implemented successful product design, development, verification, validation and manufacturing process programs for medical device companies. Kurani has held leadership positions at several leading organizations—Natera, Affymetrix, Ligand Pharmaceuticals, Kaiser Permanente, and Abbot Diagnostics—and secured regulatory and marketing approvals for medical devices and drugs from the FDA, the EU, and other global regulatory agencies.

Bharat (Bill) C Kurani
Bharat (Bill) Kurani's courses currently open for enrollment

Foundations in Medical Devices: Developing Premarket U.S. Regulatory Strategies and Working in a Regulated Environment

REGL.X410
$795
Currently no classes scheduled. Would you like to be notified when a class is available?

Foundations in Medical Devices: Developing Regulatory Strategies

REGL.X410
$795
Bharat (Bill) Kurani
Feb. 26 - Apr. 9, Thursday, 6:00pm - 9:00pm
  • Flexible Attend in person or via Zoom at scheduled times.
REGL.X410.(10)
Schedule
Date Start Time End Time Meeting Type Location
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, 03-12-2026 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, 04-02-2026 6:00pm 9:00pm Flexible SANTA CLARA / REMOTE
Thu, 04-09-2026 6:00pm 9:00pm Flexible SANTA CLARA / REMOTE
 

This class meets simultaneously in a classroom and remotely via Zoom. Students are expected to attend and participate in the course, either in-person or remotely, during the days and times that are specified on the course schedule. Students attending remotely are also strongly encouraged to have their cameras on to get the most out of the remote learning experience. Students attending the class in-person are expected to bring a laptop to each 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 Textbook:
Fundamentals of Medical Device Regulations, 5th Ed., RAPS. ISBN: 978-1-947493-80-3

Associated Program(s)
Medical Device Quality and Design
Regulatory Affairs