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draft guidance
CRO
FDA draft recommends all cancer trials collect OS data
Even when OS is not used as the primary endpoint, the FDA still advises that trial sponsors collect and submit survival data to the regulator.
Darren Incorvaia
Aug 20, 2025 10:59am
FDA issues draft guidance on clinical trial tissue biopsies
Jan 6, 2025 2:55pm
FDA releases draft guidance on clinical trial diversity
Jun 27, 2024 7:05am
FDA suggests new tests for morcellator tissue containment tools
Jun 22, 2022 6:25pm
FDA ramps up medical device cybersecurity recommendations
Apr 8, 2022 11:50am
