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Regulations & Services of PMDA
Information about Approved Products in Japan
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Information for approved products in Japan
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Development of Drugs, Medical devices, Regenerative medicines and in Vitro diagnostics
Information for approved products in Japan
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Regulations and services of PMDA
Information for approved products in Japan
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Regulations and Services of PMDA
Information for apporoved products in Japan
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Regulations and Services of PMDA
Information for apporoved products in Japan
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Reviews and Related Services
Post-marketing Safety Measures
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Reviews and Related Services
Post-marketing Safety Measures
Regulatory Science/The Science Board/Standard Development
The 2nd Subcommittee on Rare Cancers
Press Release
Date and Time: December 9, 2016 from 4pm to 6pm
Agenda / List of Handouts
Agenda
- Expectation for Drug Development for Rare Cancers –from the Clinical Site- (Dr. Akira Kawai, a Member of the Subcommittee)
- Clinical Development of Rare Cancers by Genome Analysis (Dr. Tatsuhiro Shibata, a Member of the Subcommittee)
- Points to Consider and Future Plan
- Others
List of Handouts
- Document 1 Rationale to Discuss Rare Cancers
- Document 2 Points to Consider (Chart)
- Document 3 The 1st Subcommittee Minutes Summary
- Document 4 The 1st Subcommittee Minutes Summary (Chart)
- Document 5 Lecture Materials (Dr. Akira Kawai, a Member)
- Document 6 Lecture Materials (Dr. Tatsuhiro Shibata, a Member)