Regulatory Perspective on Drug Safety Assessment during Drug Development

• In: Symposium A4: Systems pharmacology –innovative approaches to drug safety on Wednesday, 24 May 2017, 09:10-09:35
• At: Stockholm (Sweden) (2017)
• Type: Presentation
• By: SATO, Masanobu (Pharmaceuticals & Medical Devices Agency, Tokyo, Japan)
• Co-author(s): Masanobu Sato: Pharmaceuticals & Medical Devices Agency, Tokyo, Japan
  
• Abstract:

  One of the major concerns when conducting evaluation of a new drug at the Pharmaceuticals and Medical Devices Agency (PMDA) in Japan is whether there are any unacceptable risks as compared to the benefit.  A comprehensive evaluation on drug safety should be conducted considering whether the recognized risks in clinical studies can be controlled,

  ..

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. Please login