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Regulatory Science/The Science Board/Standard Development

The 4th Subcommittee on Non-clinical Studies

Press Release

Date and Time: March 11, 2015  from 10am to 12pm

Agenda / List of Handouts

Agenda
  1. Non-clinical studies from a viewpoint of the regulatory authority (PMDA)
  2. Towards summary of the past discussions
  3. Others
List of Handouts
  • Document 1-1 Cases of non-clinical pharmacology studies of oncology drugs
  • Document 1-2 Cases of non-clinical pharmacology studies of oncology drugs(Modified version of the material of #1-1 for publishing purposes)
  • Document 2 Summary outline of the discussions in the Subcommittee on Non-clinical Studies (Draft)