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Recorded Webinars

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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