Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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Webinars

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

David Nettleton
Apr 14, 2026

Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile M ....

Carolyn Troiano
Apr 14, 2026

Risk Management of Raw Materials in a GMP Environment

Barry A Friedman
Apr 16, 2026

How to write SOP's that Avoid Human Error

Ginette M Collazo
Apr 21, 2026

The New FDA QMSR (21 CFR 820): Transition Strategy & ISO 13485 Alignment

John E Lincoln
Apr 22, 2026

How to Investigate Environmental Monitoring Excursions

Gerry O Dell
Apr 22, 2026

Function, Preparation and Execution of Job Aids in the Pharmaceutical Industry

Michael Esposito
Apr 28, 2026

You have a BI Positive or Product Sterility Positive - Now What?

Gerry O Dell
Apr 28, 2026

Technical Writing - Medical Devices - Writing Effective 510K, PMA, and De Novo Submissions

Charles H Paul
Apr 29, 2026

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

David Nettleton
May 5, 2026

Latest Trends in Human Error Reduction in GMP Manufacturing

Ginette M Collazo
May 14, 2026

When Is the Evidence Enough? Probability, Risk, and Regulatory Decisions

Elaine Eisenbeisz
May 14, 2026

Seminars

Good Manufacturing Practices (GMP)

Michael Esposito
Virtual Seminar | April 16-17, 2026

21 CFR Part 11 Compliance for SaaS/Cloud Applications

David Nettleton
Virtual Seminar | April 22-23, 2026

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

David Nettleton
Virtual Seminar | April 22-23, 2026

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