Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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

David Nettleton
Feb 17, 2026

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

Gerry O Dell
Feb 18, 2026

Human Error Investigations, Root Cause Determination and CAPA Effectiveness

Ginette M Collazo
Feb 24, 2026

Process Simulation Testing for Aseptically Filled Products; An In-depth Examination of the ....

Barry A Friedman
Feb 26, 2026

FDA Guidance for Use of Social Media by Regulated Industries

Carolyn Troiano
Feb 27, 2026

Applied Time Series Analysis in Healthcare

Elaine Eisenbeisz
Mar 12, 2026

Onboarding in a GMP Environment: Best Practices for Foundational Employee Success

Michael Esposito
Mar 16, 2026

Ensuring Data Integrity and Minimizing Human Error: Practical Strategies and Tools for Suc ....

Ginette M Collazo
Mar 17, 2026

Ethylene Oxide (EO) Sterilization Basics for R&D Engineers

Gerry O Dell
Mar 19, 2026

ICH Q7A GMPs for Active Pharmaceutical Ingredients Training Course

Barry A Friedman
Mar 19, 2026

The 6 Most Common Problems in FDA Software Validation and Verification

David Nettleton
Mar 24, 2026

FDA Compliance for Regulated Systems Using COTS, Cloud & SaaS Solutions

Carolyn Troiano
Mar 27, 2026

Quality Agreements and Their Role as Part of a Quality System

Michael Ferrante
Mar 30, 2026

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

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Webinars

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

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

Human Error Investigations, Root Cause Determination and CAPA Effectiveness

Process Simulation Testing for Aseptically Filled Products; An In-depth Examination of the ....

FDA Guidance for Use of Social Media by Regulated Industries

Applied Time Series Analysis in Healthcare

Onboarding in a GMP Environment: Best Practices for Foundational Employee Success

Ensuring Data Integrity and Minimizing Human Error: Practical Strategies and Tools for Suc ....

Ethylene Oxide (EO) Sterilization Basics for R&D Engineers

ICH Q7A GMPs for Active Pharmaceutical Ingredients Training Course

The 6 Most Common Problems in FDA Software Validation and Verification

FDA Compliance for Regulated Systems Using COTS, Cloud & SaaS Solutions

Quality Agreements and Their Role as Part of a Quality System

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

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

Seminars

Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products

Verification and Validation - Product, Equipment/Process, Software and QMS : 2-Day Virtual Seminar

SOP Writing, Training and Compliance in the Pharmaceutical Industry

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Good Manufacturing Practices (GMP)

21 CFR Part 11 Compliance for SaaS/Cloud Applications

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

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