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Live Webinars

Artificial Intelligence (AI), Machine Learning (ML) and FDA Compliance for Computer Systems and Data

January 21, 2025

Carolyn Troiano $229 USD

Human Factors Engineering in Medical Device Design

January 30, 2025

Charles H. Paul $229 USD

FDA Audit Preparation Seminar

February 7, 2025

Charles H. Paul $229 USD

Verification and Validation - Product, Equipment/Process, Software and QMS

January 16, 2025

John E. Lincoln $229 USD

Trial Master File (TMF)/eTMF, and FDA's Draft Guidance for Electronic Records/Signatures Used in Clinical Trials

February 14, 2025

Carolyn Troiano $229 USD

Recorded Webinars

Technical Writing for Medical Devices

August 19, 2024

Joy McElroy $229 USD

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

December 26, 2024

David Nettleton $229 USD

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

October 29, 2024

Carolyn Troiano $229 USD

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

October 15, 2024

Carolyn Troiano $229 USD

Pharmaceutical Webinars

Live Webinars

Artificial Intelligence (AI), Machine Learning (ML) and FDA Compliance for Computer Systems and Data

Human Factors Engineering in Medical Device Design

FDA Audit Preparation Seminar

Verification and Validation - Product, Equipment/Process, Software and QMS

Trial Master File (TMF)/eTMF, and FDA's Draft Guidance for Electronic Records/Signatures Used in Clinical Trials

Recorded Webinars

Technical Writing for Medical Devices

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

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

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

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