[
フレーム]
Please make JavaScript on and see this site.
Back
-
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
Back
-
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 3rd Subcommittee on Rare Cancers
Press Release
Date and Time:February 17, 2017 from 4pm to 6pm
Agenda / List of Handouts
Agenda
- Pathophysiological Mechanism of Rare Disease Using Patient-Derived iPS Cells and Drug Discovery (Dr. Junya Toguchida, a Member of the Subcommittee)
- Study of Hematological Immunity Disorders Using iPS Cells (Dr. Toshio Heike, a Member of the Subcommittee)
- Development of Gene Therapy and Immunotherapy (Dr. Kenzaburo Tani, a Member of the Subcommittee)
- Points to Consider and Future Plan
List of Handouts
- Document 1 Responsible Party (Draft)
- Document 2 The 2nd Subcommittee Minutes Summary
- Document 3 The 1st-2nd Subcommittee Discussion Summary
- Document 4 Lecture Materials (Dr. Junya Toguchida, a Member)
- Document 5 Lecture Materials (Dr. Toshio Heike, a Member)
- Document 6 Lecture Materials (Dr. Kenzaburo Tani, a Member)