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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
Back
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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 32nd Science Board Meeting
Press Release
Date and Time: August 19, 2019 from 2pm to 4pm
Agenda / List of Handouts
Agenda
- Recent Activities of the Subcommittee on Genome Editing
- Report of Subcommittee on AMR (Draft)
- About the New Discussion Theme
- Others
List of Handouts
- Document 1 Recent Activities of the Subcommittee on Genome Editing
- Document 2-1 Report of Clinical Evaluation of Antimicrobial Agents for AMR (Draft)
- Document 2-2 Summary on Report of Clinical Evaluation of Antimicrobial Agents for AMR (Draft)
- Document 3 Point to Consider of Reviewing Medical Device Software Using Computer Simulation