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Register for access to our free webcast: ...or contact us: #pharma #deviceregulatory #riskmanagement #combinationproduct #drugdelivery #FDA #regulatoryaffairs Max Lerman, PhD Sarah Mollo Rob Schulz BlueRidge Life Sciences To view or add a comment, sign in The FDA has taken a step toward greater transparency and efficiency in drug development by publishing the internal filing checklists used by CDER reviewers

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Menstrual changes are not considered a common side effect of GLP-1s

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May 1, 2026: Judge in Ozempic MDL Issues Two Discovery Orders as Number of NAION Claims Approaches 90 There are 86 claims in the multidistrict litigation about whether Ozempic and other GLP-1s caused some patients to develop NAION