Regulatory and Compliance training at reasonable prices!

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Live Webinars

Recorded Webinars

Monday
June
14
2021

6-Hour Virtual Seminar on Biostatistics for the Non- ...

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

Duration: 6 Hours

Speaker: Elaine Eisenbeisz View Details

Tuesday
June
15
2021

ISO13485: 2016 - Quality Management Systems for ...

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

Duration: 90 Minutes

Speaker: Yuval Shapiro View Details

Tuesday
June
15
2021

Good Manufacturing Practices (GMP) - An Intr ...

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

Duration: 90 Minutes

Speaker: Michael Esposito View Details

Wednesday
June
16
2021

Water System Biofilm Control and Microbial Monitorin ...

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

Duration: 90 Minutes

Speaker: Teri C. Soli View Details

Thursday
June
17
2021

How to Prepare for and Host an FDA Inspection and re ...

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

Duration: 60 Minutes

Speaker: Edwin Waldbusser View Details

View All

Recorded Webinars

Joy McElroy | View Anytime | 6 Hours

6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)

Carolyn Troiano | View Anytime | 90 Minutes

Computer System Validation (CSV) for FDA-Regulated Computers

Ginette Collazo | View Anytime | 60 Minutes

Human Error Reduction in GMP Related Environments

Charles H. Paul | View Anytime | 60 Minutes

Preventing Human Error in the Life Sciences

Martin K. Behr, III | View Anytime | 90 Minutes

INCOTERMS 2020 Made Easy - Decoding your Shipment

Regulatory and Compliance training at reasonable prices!

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

Live Webinars

Recorded Webinars

6-Hour Virtual Seminar on Biostatistics for the Non- ...

ISO13485: 2016 - Quality Management Systems for ...

Good Manufacturing Practices (GMP) - An Intr ...

Water System Biofilm Control and Microbial Monitorin ...

How to Prepare for and Host an FDA Inspection and re ...

Recorded Webinars

6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)

Computer System Validation (CSV) for FDA-Regulated Computers

Human Error Reduction in GMP Related Environments

Preventing Human Error in the Life Sciences

INCOTERMS 2020 Made Easy - Decoding your Shipment

Importing and Exporting Covid-19 Products

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