Jan
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jan 9, 2025
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Michael Ferrante
How to conduct an effective BSA Audit
Jan 10, 2025
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Justin Muscolino
Supplier Management with the new Medical Device Regulation EU MDR 745/2017
Jan 13, 2025
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Frank Stein
Troubleshooting Ethylene Oxide (EO) Processes
Jan 13, 2025
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Gerry O Dell
Preapproval Inspection and Submission to the FDA
Jan 14, 2025
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John E Lincoln
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Man ....
Jan 15, 2025
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Roger Cowan
Supply Chain and Product Compliance Using RoHS, REACH, and Conflict Minerals
Jan 15, 2025
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Kelly Eisenhardt
Feb
Calibration and Validation of Equipment
Feb 4, 2025
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John E Lincoln
Function, Preparation and Execution of Job Aids in the Pharmaceutical Industry
Feb 4, 2025
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Michael Esposito
Trial Master File and Clinical Data Management Regulated by FDA
Feb 5, 2025
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Carolyn Troiano
Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR
Feb 5, 2025
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David Nettleton
EU Medical Device Regulation 2017/745
Feb 6, 2025
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Juan M Campos
Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Enviro ....
Feb 10, 2025
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Gerry O Dell
Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
Feb 10, 2025
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Joy McElroy
Mar
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