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  Regulatory Sciences (RS) Section


RS LogoThe RS Section of the American Association of Pharmaceutical Scientists (AAPS) is composed of members whose interests focus on multidisciplinary scientific aspects of pharmaceutical development and regulatory approval as they relate to quality, safety and efficacy of the product (e.g., manufacturing, quality, pharmacology, toxicology, clinical trials, law, and intellectual property).

MEMBERSHIP BENEFITS
  • Gain knowledge of regulatory science and policies.
  • Be current on complex regulatory issues in drug development.
  • Attend and participate in symposiums and workshops sponsored by the RS section.
  • Provide input into the programs/activities.
  • Network with the members of AAPS and other organizations.
  • Gain access to leadership opportunities across a variety of RS-sponsored activities.
2009 Membership Meeting Presentation

2009 Awards Presentation


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Read the new July 2009 RS Section Newsletter!

Archived RS Section Newsletters


Regulatory Sciences Headlines

Evaluation of Post-Authorization Safety Studies in the First Cohort of EU Risk Management Plans at Time of Regulatory Approval
Drug Safety (12/10) Vol. 32, No. 12, P. 1175; Giezen, Thijs J.; Mantel-Teeuwisse, Aukje K.; Straus, Sabine M.J.M; et al.

FDA Drug Safety Communication: Ongoing Review of Rosiglitazone and Cardiovascular Safety
FDA.gov (02/22/10)

'FDA Announces New Safety Plan for Agents Used to Treat Chemotherapy-Related Anemia' and 'Drug Safety Communication: ESAs...'
FDA.gov (02/16/10)

U.S. Clears Wider Use of AstraZeneca Cholesterol Drug
Reuters (02/08/10) Richwine, Lisa

The European Medicine Agency Road Map to 2015: The Agency's Contribution to Science, Medicines, Health
European Medicines Agency (01/26/2010)

All Headlines
RS, FDA, and EMEA News



RS Section Important Dates
MONTH EVENT LOCATION CONTACT
March 2010
12 Section Election Slates Due Karol Shadle
16 NBCPC Conference Call 12:00pm (Noon) EST Sharon Pichon
17 EC Conference Call 2:00 pm EST Karol Shadle


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