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Drugs
Webinar
Jul 11, 2024
–
Jul 11, 2024
Postmarket Surveillance in the Real World: The FDA’s Perspective on RWD/RWE
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Webinar
Jun 20, 2024
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Jun 20, 2024
Inspection Readiness for EU GMP Annex 1 – Manufacture of Sterile Medicinal Products
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Webinar
Jun 13, 2024
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Jun 13, 2024
FDA in 2024 and Beyond: What Election-Year Changes Mean for Your Business
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Webinar
May 30, 2024
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May 30, 2024
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule
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FDA, FTC and DOJ Enforcement of Medical Device Regulations
Using Real-World Evidence in Drug and Device Submissions
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Draft Guidance Covers Using URRAs in Combo Product Applications
The Revised ICH E8:
A Guide to New Clinical Trial Requirements
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