1) Rationale for the change
Not specified for this version.
Detailed Commission guideline of 8 December 2017 on the good manufacturing practice for investigational medicinal products pursuant to the second paragraph of the Article 63(1) of Regulation (EU) No 536/2014
Version 2017-12-08
- Publication
- Dec 8, 2017
- Effective Date
- -
- Filename
- a0b206a0-5788-406b-9e20-e0525b16e712_en
- Checksum
- 57882e9538660fea332ad7a57b7b6fb885d9e6f4cf79284487885bdf3bdcf688
Change Summary
Imported from European Commission — EudraLex source page.
Version Change Summary
2) To whom it applies
Not specified for this version.
4) The current change description
Not specified for this version.
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