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The 3rd Term Science Board (FY2016, FY2017)

The 3rd Term Science Board Member List

Date	No.	PressRelease	Agenda/List of Handouts	Minutes
March 9, 2018	26th mtg.	PressRelease	Agenda/List of Handouts	Minutes
January 12, 2018	25th mtg.	PressRelease	Agenda/List of Handouts	Minutes
November 13, 2017	24th mtg.	PressRelease	Agenda/List of Handouts	Minutes
September 22, 2017	23rd mtg.	PressRelease	Agenda/List of Handouts	Minutes
May 12, 2017	22nd mtg.	PressRelease	Agenda/List of Handouts	Minutes
January 13, 2017	21st mtg.	PressRelease	Agenda/List of Handouts	Minutes
November 25, 2016	20th mtg.	PressRelease	Agenda/List of Handouts	Minutes
November 11, 2016	19th mtg.	PressRelease	Agenda/List of Handouts	Minutes
September 12, 2016	18th mtg.	PressRelease	Agenda/List of Handouts	Minutes
July 8, 2016	17th mtg.	PressRelease	Agenda/List of Handouts	Minutes
May 27, 2016	16th mtg.	PressRelease	Agenda/List of Handouts	Minutes

Regulatory Science/The Science Board/Standard Development

Regulatory Science
The Science Board
- Outline
- The Science Board
- Subcommittees
  - Subcommittee on Cell and Gene Therapy Products Produced in vivo
  - Subcommittee on Therapeutic Products Based on Extracellular Vesicles (EVs) Including Exosomes
  - Subcommittee on Microbiome
  - Subcommittee on AMR
  - Subcommittee on Rare Cancers
  - Subcommittee on Pharmaceuticals Development
  - Subcommittee on Placebo-controlled Studies
  - Subcommittee on Non-clinical Studies
  - Pharmaceuticals Subcommittee
  - Bio-products Subcommittee
  - Subcommittee on Software as a Medical Device Utilizing AI and Machine Learning
  - Subcommittee on Computer Simulation
  - Subcommittee on AI (Artificial Intelligence)
  - Subcommittee on Application of Numerical Analysis to Non-clinical Evaluation
  - Subcommittee on Evaluation of Medical Devices in Pediatric Use
  - Medical Devices Subcommittee
  - Subcommittee on Genome Editing
  - CPC (Cell Processing Center) Subcommittee
  - Cellular and Tissue-based Products Subcommittee
Standard Development

Pmda - Pharmaceuticals and Medical Devices Agency

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