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Medical Devices
Compliance with 21 CFR Part 11; Data integrity for SaaS/Cloud, EU G...
David Nettleton
Sep 23, 2019 - 01:00 PM EDT
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Hospital & Healthc..
10 Tips for Successful Hospital Utilization Management: From Founda...
Beverly Cunningham
Sep 23, 2019 - 01:00 PM EDT
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Pharmaceutical
Bioanalytcial sample re-analysis, ISR and analytical re-analysis
Edward 'O' Connor
Sep 23, 2019 - 01:00 PM EDT
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Pharmaceutical
3-Hour Virtual Seminar: Validation Challenges for Bioassays
Gwendolyn Wise-Blackman
Sep 24, 2019 - 01:00 PM EST
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Hospital & Healthc..
Introduction to Combination Products: Navigating The Rules and Regu...
Dr. Ginette Collazo
Sep 24, 2019 - 01:00 PM EST
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Pharmaceutical
Auditing for Microbiological Aspects of Pharmaceutical and Biopharm...
Carl Patterson
Sep 24, 2019 - 01:00 PM EDT
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Pharmaceutical
Quality Risk Management Overview for Pharma, Biopharma and Combinat...
Marina Malikova
Sep 24, 2019 - 01:00 PM EDT
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Pharmaceutical
Comparability Protocols For Approved Drugs
Peggy J Berry
Sep 24, 2019 - 01:00 PM EDT
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Medical Devices
The Use and Misuse Of FMEA In Medical Device Risk Management
Dev R.
Sep 24, 2019 - 01:00 PM EST
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Pharmaceutical
Gaining and Re-establishing Control of your Cleanroom
Joy L. McElroy
Sep 26, 2019 - 01:00 PM EST
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Food Safety & Diet..
FDA NLEA Regulation for Retail and Foodservice Labeling An Overvie...
Natasha Rowley-Phipps
Sep 26, 2019 - 01:00 PM EST
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Clinical Trial
Trial Master File (TMF): FDA Expectations From Sponsors and Sites
Marina Malikova
Sep 26, 2019 - 01:00 PM EST
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Medical Devices
The 510(K) Submission: Requirements, Contents, and Options
Jeff Kasoff
Sep 27, 2019 - 01:00 PM EDT
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Pharmaceutical
Validation of Trace-Level Analyses for Impurities and Degradation P...
John C. Fetzer
Sep 27, 2019 - 01:00 PM EDT
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Pharmaceutical
Orphan Drug Development History & Overview
Joy L. McElroy
Sep 27, 2019 - 02:00 PM EDT
