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Quicksand | Episode 49

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Manage episode 217996709 series 2359978
Content provided by Robert Cormack. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Robert Cormack or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.

DEA reclassifies CBD-containing Epidiolex as Schedule V drug; FDA releases draft guidance on human factors studies; FDA releases draft guidance documents on adaptive clinical trials and master protocols; Study estimates average cost of Phase 3 studies at $19 million; MHRA permits use of eConsent for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

  continue reading

20 episoade

Artwork
iconDistribuie
 
Manage episode 217996709 series 2359978
Content provided by Robert Cormack. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Robert Cormack or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.

DEA reclassifies CBD-containing Epidiolex as Schedule V drug; FDA releases draft guidance on human factors studies; FDA releases draft guidance documents on adaptive clinical trials and master protocols; Study estimates average cost of Phase 3 studies at $19 million; MHRA permits use of eConsent for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

  continue reading

20 episoade

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