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Quicksand | Episode 49
Manage episode 217996709 series 2359978
DEA reclassifies CBD-containing Epidiolex as Schedule V drug; FDA releases draft guidance on human factors studies; FDA releases draft guidance documents on adaptive clinical trials and master protocols; Study estimates average cost of Phase 3 studies at $19 million; MHRA permits use of eConsent for clinical trials
20 episodios
Manage episode 217996709 series 2359978
DEA reclassifies CBD-containing Epidiolex as Schedule V drug; FDA releases draft guidance on human factors studies; FDA releases draft guidance documents on adaptive clinical trials and master protocols; Study estimates average cost of Phase 3 studies at $19 million; MHRA permits use of eConsent for clinical trials
20 episodios
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