Overview

RS 


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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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Announcements

AAPS Fellow nominations are due April 29, 2016. 

Apply for awards and travelships recognized at the 2016 AAPS Annual Meeting and Exposition. Applications are due June 15, 2016. 

Submit your contributed paper abstract to the 2016 AAPS Annual Meeting and Exposition by June 15, 2016. Read the RS Section Helpful Hints Flyer (PDF) to learn more about submitting your paper to the RS section. 

The RS section is seeking a Discussion Group Liaison volunteer. To volunteer, please contact Monica Whitmire for details.

AAPS eCourses
 - Regulatory Affairs 101 
 - Good Oral Candidates 101 
 - Stability Testing 101 

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Events