Regulatory Aspects of Cell and Gene Therapy Products: The Japanese Perspective-Reference-Cited by-同舟云学术

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Regulatory Aspects of Cell and Gene Therapy Products: The Japanese Perspective

Published:2023 Issue: Volume: Page:155-179
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
Short-container-title:

Author:

Maruyama Yoshiaki,Noda Shinichi,Okudaira Shinichi,Sakurai Akira,Okura Narumi,Honda Futaba

Publisher

Springer International Publishing

Link

https://link.springer.com/content/pdf/10.1007/978-3-031-34567-8_9

Reference68 articles.

1. The Act on the Safety of Regenerative Medicine, Act No. 85, 2013. [in Japanese]. https://elaws.e-gov.go.jp/document?lawid=425AC0000000085_20190314_430AC0000000098

2. Pharmaceuticals, Medical Devices and Other Therapeutic Products Act (Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices), Act No. 145, 1960. [in Japanese/English]. https://www.japaneselawtranslation.go.jp/en/laws/view/3213

3. Medical practitioners’ Act, Act No. 201, 1948. [in Japanese/English]. https://www.japaneselawtranslation.go.jp/ja/laws/view/3992

4. Medical Care Act, Act No. 205, 1948. [in Japanese/English]. https://www.japaneselawtranslation.go.jp/en/laws/view/4006

5. Policy information. https://www.mhlw.go.jp/english/policy/health-medical/medical-care/dl/150407-01.pdf

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1. Regulatory Aspects of Regenerative Medicine in the United States and Abroad;Dermatological Reviews;2024-08

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