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Recorded Webinars

Thursday
May
15
2025

The Human Error Toolbox: A Practical Approach to ...

Time: 10:00 AM PDT | 01:00 PM EDT

Duration: 90 Minutes

Speaker: Ginette Collazo View Details

Thursday
May
15
2025

Risk-Based Validation of Spreadsheet Applications

Time: 10:00 AM PDT | 01:00 PM EDT

Duration: 90 Minutes

Speaker: Carolyn Troiano View Details

Thursday
May
15
2025

Excel Meets AI - How Microsoft Copilot Can Save You ...

Time: 10:00 AM PDT | 01:00 PM EDT

Duration: 60 Minutes

Speaker: Mike Thomas View Details

Thursday
May
15
2025

EU Medical Device Regulation (MDR) - Updated ...

Time: 10:00 AM PDT | 01:00 PM EDT

Duration: 90 Minutes

Speaker: Robert J. Russell View Details

Thursday
May
15
2025

Project Scheduling Techniques for Medical Device Sub ...

Time: 10:00 AM PDT | 01:00 PM EDT

Duration: 60 Minutes

Speaker: Charles H. Paul View Details

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Recorded Webinars

Gina Reo | View Anytime | 60 Minutes

Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes

Roger Cowan | View Anytime | 60 Minutes

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Roger Cowan | View Anytime | 60 Minutes

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

Roger Cowan | View Anytime | 60 Minutes

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture

Roger Cowan | View Anytime | 75 Minutes

HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms

Roger Cowan | View Anytime | 60 Minutes

Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

View All

Regulatory and Compliance training at reasonable prices!

Out of the world training at down-to-earth prices

Live Webinars

Recorded Webinars

The Human Error Toolbox: A Practical Approach to ...

Risk-Based Validation of Spreadsheet Applications

Excel Meets AI - How Microsoft Copilot Can Save You ...

EU Medical Device Regulation (MDR) - Updated ...

Project Scheduling Techniques for Medical Device Sub ...

Recorded Webinars

Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture

HVAC and GMP Environmental Control for Pharmaceutical Clean Rooms

Pharmaceutical Compressed Air - Quality GMP Standards and Requirements

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