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Commentary on the EMA Guideline on strategies to identify and mitigate risks for first-in-human and early clinical trials with investigational medicinal products (EMEA/CHMP/SWP/28367/07 Rev. 1.
7 May 2018. doid: 10.1111/bcp.13550
van Gerven J, Bonelli M
View publicationCommentary on the EMA Guideline on strategies to identify and mitigate risks for first‐in‐human and early clinical trials with investigational medicinal products (EMEA/CHMP/SWP/28367/07 Rev. 1
Advancing the boundaries of clinical drug development
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