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Recorded Webinars

Cybersecurity - The Latest US FDA Requirements

John E. Lincoln

Cybersecurity - The Latest US FDA Requirements

Pharmaceuticals

Broadcast Date

90 Minutes

Apr 03, 2026

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Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies

John E. Lincoln

Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies

Pharmaceuticals

Broadcast Date

90 Minutes

Mar 19, 2026

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ChatGPT / AI for Project Management for FDA-Regulated Companies

John E. Lincoln

ChatGPT / AI for Project Management for FDA-Regulated Companies

Pharmaceuticals

Broadcast Date

60 Minutes

Mar 13, 2026

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FDA New Software Validation Requirements

John E. Lincoln

FDA New Software Validation Requirements

Pharmaceuticals

Broadcast Date

90 Minutes

Mar 05, 2026

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Risk Management for AI in Medical Devices: Insights from FDA Lifecycle Management Draft Guidance

John E. Lincoln

Risk Management for AI in Medical Devices: Insights from FDA Lifecycle Management Draft Guidance

Pharmaceuticals

Broadcast Date

90 Minutes

Mar 04, 2026

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Human Error Prevention (HEP) - Risk Factors and Strategies

John E. Lincoln

Human Error Prevention (HEP) - Risk Factors and Strategies

Pharmaceuticals

Broadcast Date

240 Minutes

Mar 03, 2026

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Latest Trends in Human Error Reduction in GMP Manufacturing: Strategies for Compliance and Operational Excellence

Ginette Collazo

Latest Trends in Human Error Reduction in GMP Manufacturing: Strategies for Compliance and Operational Excellence

Pharmaceuticals

Broadcast Date

90 Minutes

Oct 23, 2025

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Lifecycle and Validation of Analytical Procedures FDA ICH and USP

Lifecycle and Validation of Analytical Procedures FDA ICH and USP

Pharmaceuticals

Broadcast Date

60 Minutes

Oct 09, 2025

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Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA

Carolyn Troiano

Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA

Pharmaceuticals

Broadcast Date

90 Minutes

Nov 25, 2024

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Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

David Nettleton

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Pharmaceuticals

Broadcast Date

90 Minutes

Sep 26, 2024

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3-Hour FDA Audit Preparation Virtual Seminar

Charles H. Paul

3-Hour FDA Audit Preparation Virtual Seminar

Pharmaceuticals

Broadcast Date

180 Minutes

Aug 26, 2024

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21 CFR Part 11, FDA Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

Carolyn Troiano

21 CFR Part 11, FDA Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA

Pharmaceuticals

Broadcast Date

90 Minutes

Aug 12, 2024

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FDA Best Audit Practices – Get Ready For The Inspection That Is Coming

Charles H. Paul

FDA Best Audit Practices – Get Ready For The Inspection That Is Coming

Pharmaceuticals

Broadcast Date

120 Minutes

Jun 26, 2024

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Corrective and Preventive Action (CAPA): Our Most Important Quality Process

William A. Levinson

Corrective and Preventive Action (CAPA): Our Most Important Quality Process

Pharmaceuticals

Broadcast Date

90 Minutes

Jun 05, 2024

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Understand and Apply ISO New Climate Change Requirements

William A. Levinson

Understand and Apply ISO New Climate Change Requirements

Pharmaceuticals

Broadcast Date

90 Minutes

May 21, 2024

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