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Unleashing Excellence in Quality, Supply Chain, HPAPIs & Orphan Drugs.
Released By Curia
October 9, 2023
FDA’s Quality Management Maturity Program Why should CDMOs adhere to the new CDER’s Rating System? Read More >> FDA 2023 Inspection Roadmap Is “Readiness” in your annual objectives? Read More >> The Shift Toward US Pharmaceutical Manufacturing Considerations in attaining the right global mix. Read More >> HPAPI Development & Manufacturing Trends Safety, containment, and analysis of the highly potent compounds from development to commercialization. Read More >> Orphan Drug Development: A Pragmatic Approach to Developing a Rare Disease Drug Challenges and considerations associated with the expedited development of orphan drugs, and how to successfully work through them. Read More >> Orphan Drug Designation in the US: Why does it matter Investigating how and why small pharmas should get onboard to help develop medicines effective in the treatment of orphan diseases. Read More >>
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