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Friday
November
07
2025

Excel - Reporting Simplified - Learn Pivot Tables from Scratch

Time: 11:00 AM PST | 02:00 PM EST

Duration: 60 Minutes

Speaker: Mike Thomas View Details

Friday
November
07
2025

4-Hour Virtual Seminar on Credit Risk Management- Principles and Practices, Tools and Techniques

Time: 08:00 AM PST | 11:00 AM EST

Duration: 4 Hours

Speaker: Dev Strischek View Details

Friday
November
07
2025

Device Changes, FDA Changes, and the 510(K)

Time: 11:00 AM PST | 02:00 PM EST

Duration: 90 Minutes

Speaker: John E Lincoln View Details

Friday
November
07
2025

6-Hour Virtual Seminar on The EU Clinical Trial Regulation - EU Filings & Registrations

Time: 08:00 AM PST | 11:00 AM EST

Duration: 6 Hours

Speaker: John E Lincoln View Details

Friday
November
07
2025

Variance Analysis for Busy Managers: Budget vs Actuals Made Simple

Time: 09:00 AM PST | 12:00 PM EST

Duration: 60 Minutes

Speaker: Justin Muscolino View Details

Friday
November
07
2025

Using a Learning Management System (LMS) to Develop Pharma Training Curricula

Time: 11:00 AM PST | 02:00 PM EST

Duration: 90 Minutes

Speaker: Michael Esposito View Details

Monday
November
10
2025

How to Use Copilot For MS Project

Time: 10:00 AM PST | 01:00 PM EST

Duration: 60 Minutes

Speaker: Tom Fragale View Details

Monday
November
10
2025

EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations

Time: 12:00 PM PST | 03:00 PM EST

Duration: 90 Minutes

Speaker: Robert J. Russell View Details

Regulatory and Compliance training at reasonable prices!

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

Live Webinars

Excel - Reporting Simplified - Learn Pivot Tables from Scratch

4-Hour Virtual Seminar on Credit Risk Management- Principles and Practices, Tools and Techniques

Device Changes, FDA Changes, and the 510(K)

6-Hour Virtual Seminar on The EU Clinical Trial Regulation - EU Filings & Registrations

Variance Analysis for Busy Managers: Budget vs Actuals Made Simple

Using a Learning Management System (LMS) to Develop Pharma Training Curricula

How to Use Copilot For MS Project

EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations

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