Regulatory framework in clinical research
- In: C3 - Clinical research on Tuesday, 6 September 2011, 09:00-12:00
- At: Hyderabad (India) (2011)
- Type: Presentation
- By: YACOBI, Avraham (Taro Pharmaceuticals, New York, United States of America)
- Co-author(s): Shah, Vinod P. (FIP Scientific Secretary, The Hague, United States of America)
The regulatory framework for carrying out clinical research requires ethical considerations and great deal of skills and experience. This is exemplified with the example of development and evaluation of multiple source topical dermatological drug products. Topical drug products are administered for either systemic effects or for local action in.. The access to the whole abstract and if available the presentation file is available to FIP members and to congress participants of that specific congress.
Last update 4 October 2019