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Medical Devices
Adapting Project Management to the CGMP Environment
John E. Lincoln
Oct 29, 2019 - 01:00 PM EDT
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Pharmaceutical
USDA New Proposed Rule on BioEngineered (GMO) Food Disclosure
John Ryan
Oct 30, 2019 - 01:00 PM EDT
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Pharmaceutical
Transfer of Analytical Methods according to USP <1224>
Dr. Ludwig Huber
Oct 31, 2019 - 01:00 PM EDT
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Pharmaceutical
Cannabinoids as Drugs -- Where do we stand today?
Loren Gelber
Oct 31 - Oct 31 , 2019
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Pharmaceutical
3-hr Virtual Seminar: Bioanalytical Method Validation
Gwendolyn Wise-Blackman
Oct 31, 2019 - 01:00 PM EST
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$ 349
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Best Practices and Potential Pitfalls for Validating Computer Syste...
Carolyn Troiano
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FDA's Expectations from Supplier Management for GMP: Quality Agreem...
Danielle DeLucy
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How to Deal with the Contradictions and Challenges of Using Cloud i...
Angela Bazigos
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Using Excel Spreadsheets in FDA Regulated Environment.
Mukesh Kumar
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Studies to Support Temperature Excursions and Shipping Of Pharmaceu...
Kim Huynh-Ba
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How to Approach Organizational Change Management When Automating Pr...
Dennis Weissman
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How to write SOP's that Avoid Human Error
Ginette M Collazo
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$ 349
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Pharmaceutical
Technical Writing in the Pharmaceutical Industry
Robert Peoples
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$ 349
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Clinical Trial
The 11 Must-Have Documents Of software Verification and Validation
John E. Lincoln
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$ 349
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Pharmaceutical
