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Recorded Webinars

Monday
October
03
2022

Current Trends in FDA Compliance and Enforcement&nbs ...

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

Duration: 90 Minutes

Speaker: Carolyn Troiano View Details

Tuesday
October
04
2022

Excel: Tips and Tricks and Shortcuts

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

Duration: 60 Minutes

Speaker: Tom Fragale View Details

Tuesday
October
04
2022

6-Hour Virtual Seminar on Audit like the FDA

Time: 08:00 AM PDT | 11:00 AM EDT

Duration: 6 Hours

Speaker: Susanne Manz View Details

Tuesday
October
04
2022

3-Hour Virtual Seminar on Mastering Excel Pivot Tabl ...

Time: 09:00 AM PDT | 12:00 PM EDT

Duration: 3 Hours

Speaker: Dennis Taylor View Details

Tuesday
October
04
2022

How to Write SOP's that Avoid Human Error

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

Duration: 90 Minutes

Speaker: Ginette Collazo View Details

View All

Recorded Webinars

Gina Reo | View Anytime | 60 Minutes

Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes

Nada Kuganathan | View Anytime | 90 Minutes

Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry

Roger Cowan | View Anytime | 60 Minutes

GMP Environmental Monitoring in Pharmaceutical Clean Rooms

Roger Cowan | View Anytime | 60 Minutes

CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture

Roger Cowan | View Anytime | 60 Minutes

Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements

Roger Cowan | View Anytime | 60 Minutes

Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards

View All

Regulatory and Compliance training at reasonable prices!

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

Live Webinars

Recorded Webinars

Current Trends in FDA Compliance and Enforcement&nbs ...

Excel: Tips and Tricks and Shortcuts

6-Hour Virtual Seminar on Audit like the FDA

3-Hour Virtual Seminar on Mastering Excel Pivot Tabl ...

How to Write SOP's that Avoid Human Error

Recorded Webinars

Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes

Establishing an Effective & Pragmatic Vendor Qualification Program for cGMP Compliance in the Pharmaceutical Industry

GMP Environmental Monitoring in Pharmaceutical Clean Rooms

CMO Supplier Quality Agreements - What you need to know to comply with new FDA & EU GMP Guidelines for Contract Drug Manufacture

Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements

Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards

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