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Regulations & Services of PMDA
Information about Approved Products in Japan
Information for approved products in Japan
Development of Drugs, Medical devices, Regenerative medicines and in Vitro diagnostics
Information for approved products in Japan
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
Regulations and Services of PMDA
Information for apporoved products in Japan
Reviews and Related Services
Post-marketing Safety Measures
Reviews and Related Services
Post-marketing Safety Measures
Regulatory Science/The Science Board/Standard Development
The 35th Science Board Meeting
Press Releaseopen close
Date and Time: December 10, 2019 from 2pm to 4pm
Agenda / List of Handouts
Agenda
Report (Draft) of the Subcommittee on Genome Editing
About the New Discussion Theme
Others
List of Handouts
Document 1 Report (Draft) of the Subcommittee on Genome Editing (Points to Consider of Quality and Safety of Therapeutic Products Using Genome Editing Technology)
Document 2 Summary of Report (Draft) of the Subcommittee on Genome Editing
Document 3 The New Discussion Theme (Draft)
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