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The 6 Most Common Problems in Computer System Assurance and Validation
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2025-04-16 |
Pharmaceutical |
Recorded Webinar |
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Mastering the FDA 510(k) Submission Process: A Practical Guide
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2025-05-14 |
Pharmaceutical |
Recorded Webinar |
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Future of AI in Regulatory and Good Manufacturing Practice (GMP) in Pharma, Biotech, and Medical Device Industries
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2025-05-20 |
Pharmaceutical |
Recorded Webinar |
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Vendor Audit Best Practices for FDA-Regulated Computer Systems in Cloud Environments and Using (SaaS) Solutions
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2025-05-16 |
Pharmaceutical |
Recorded Webinar |
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Business Process Mapping: Streamlining Management of Data/Records for a Clinical Trial
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2025-05-02 |
Pharmaceutical |
Recorded Webinar |
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HVAC and GMP Environmental Control - for Pharmaceutical Clean Rooms 2025
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2025-05-29 |
Pharmaceutical |
Recorded Webinar |
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Validation of an FDA-Regulated System that Includes Artificial Intelligence (AI) and Machine Learning (ML)
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2025-06-09 |
Pharmaceutical |
Recorded Webinar |
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Computer Software Assurance: Risk-Based Validation With Time-Saving Templates in 2025
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2025-06-24 |
Pharmaceutical |
Recorded Webinar |
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