A career in regulatory affairs can take many paths, such as clinical trials, drug development, food safety, medical device advancement, pharmaceutical research, or manufacturing controls. Just knowing the fundamentals of regulatory affairs is not enough to advance a career or secure a job of some seniority in this industry.
As in most regulated industries experience alone is not sufficient, because professionals are only exposed in their jobs to a small fraction of all the cases that are being decided by the regulatory agency. To make progress in the field, a regulatory affairs professional needs periodic training and education.
This program, which grew from demands by local biotech professionals, offers a curriculum that compliments the rapidly expanding pace in the pharmaceutical and biotechnology industries, and is designed for regulatory and quality professionals who need to keep up-to-date with the latest developments and have a deeper understanding of the more complex regulatory challenges.
Our knowledgeable team of instructors includes executive level regulatory professionals and consultants with more than 20 years’ experience in quality and compliance with U.S. FDA and ICH requirements. With this breadth and depth of experience, instructors expose students to many real workplace examples.
There will be a $60 fee upon acceptance into the program
From the 'Apply Now' button, login to your student account, complete the online application, and pay the application fee if applicable.
It is preferable that you create an account before proceeding if you have not already done so.
Candidates are encouraged to apply in the certificate program as early as possible to take advantage of program benefits.
See Certificate FAQs for more information.
Science & Technology. Call 858-534-9353 or Email: firstname.lastname@example.org
Applicants to this program must have completed either the Regulatory Affairs Essentials certificate, a master’s degree from reputable institution or have at least three years’ experience working in the field.
Shiba Biotechnology Inc
Regulatory Liaisons, LLC.
UCSD Health Sciences Research Compliance Program
Katie Smith Consulting
VP Quality Assurance
Director, Regulatory Affairs
Halozyme Therapeutics, Inc.
There will be a $60 fee upon
acceptance into the program
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