The Regulatory Sciences (RS) section focuses on providing its members with the tools, programming, and networking opportunities needed to help them grow in areas such as regulatory compliance, GMP, clinical and pre-clinical practices; the legal aspects of pharmaceutical development; and protection of intellectual property. Our membership is composed primarily of professionals who practice regulatory affairs in the pharmaceutical and biopharmaceutical industries, academia, and health authorities. We collaborate with other AAPS sections, sister organizations, and regulators to inform pharmaceutical scientists of the global regulatory landscape and help shape global regulatory strategies. RS section members are involved with all aspects of drug development—from discovery through life cycle management—and place a special emphasis of continuous learning and training in accomplishing their objectives.
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