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Regulatory Requirements for Conducting an OOS Investigation
Danielle DeLucy
LIVE : October 27 , 2026 01:00 PM EDT
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory
Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in o...
Showing 1-10 of 705 items.
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HVAC and GMP Environmental Control for Pharmaceutical Cleanrooms
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical
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Pharmaceutical Compressed Air - Quality GMP Requirements - Meet FDA and International Quality Standa...
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical
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Understanding and Implementing a Technology Transfer Process
Steven Laurenz
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical | Biotchnology | Laboratory
Steven Laurenz has over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. He is skilled i...
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6-Hour Virtual Seminar on Computer System Validation for Cloud and COTS Applications
Carolyn Troiano
Recorded Duration : 360 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated indust...
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CMO Supplier Quality Agreements - Comply with new FDA & EU GMP Guidelines for Contract Drug Manufact...
Recorded Duration : 60 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
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GMP Environmental Monitoring in Pharmaceutical Clean Rooms
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical
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21 CFR Part 11 - Electronic Record and Signature Validation
Edwin Waldbusser
Recorded Duration : 60 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Ed retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. He was involved in the development ...
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GMP Auditing for Pharmaceutical Manufacturing
Carl Patterson, MS, SSGB, SSBB
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance professional who is based in San Diego, Ca...

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2-hr Virtual Seminar: Anti-Kickback, Fraud, Stark, and Marketing - Where are the Landmines?
William Mack Copeland
Recorded Duration : 120 Minutes
Life Sciences > Healthcare

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Developing & Managing a Trial Master File for FDA-Regulated Clinical Testing
Carolyn Troiano
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory
Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated indust...
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