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The Most Common Problems in FDA Software Validation & Verification
John E. Lincoln
LIVE : July 09 , 2025 01:00 PM EDT
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

John E. Lincoln, is Principal of J. E. Lincoln and Associates LLC, a consulting company with over 38 years experience in U.S. FDA-regulated ind...

Showing 691-700 of 705 items.
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New Joint Commission Requirements for Hospitals on Healthcare Technology Management
Dev Raheja
Recorded Duration : 60 Minutes
Life Sciences > Healthcare
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies ev...
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Addressing Non-Conformances by Root Cause Analysis
Michael Brodsky
Recorded Duration : 60 Minutes
Life Sciences > Laboratory

Michael has a post-graduate degree from the University of Toronto, School of Hygiene and Tropical Medicine and been an Environmental Microbiolo...

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Addressing Non-Conformances by Root Cause Analysis
Michael Brodsky
Recorded Duration : 60 Minutes
Life Sciences > Laboratory

Michael has a post-graduate degree from the University of Toronto, School of Hygiene and Tropical Medicine and been an Environmental Microbiolo...

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Regulations on Purchasing Controls for Medical Devices
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
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Trial Master File (TMF): Meeting FDA Expectations
Carolyn Troiano
Recorded Duration : 90 Minutes
Life Sciences > Clinical Trial
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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The Disruptive Practitioner: A Danger to the Hospital's Operation
William Mack Copeland
Recorded Duration : 60 Minutes
Life Sciences > Healthcare

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3-hr Virtual Seminar: Developing Documents and Records to Meet the Requirements of ISO,IEC 17025
Michael Brodsky
Recorded Duration : 60 Minutes
Life Sciences > Laboratory

Michael has a post-graduate degree from the University of Toronto, School of Hygiene and Tropical Medicine and been an Environmental Microbiolo...

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Software Validation & Testing – Regulatory Requirements
Dev Raheja
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies ev...
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Getting Ready for an FDA Inspection
Felicia Angus
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical
Felicia Angus is passionate quality professional with over 23 years of pharmaceutical experience in the clinical, solid dosage, API, sterile and biological industries and over...
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21 CFR Part 11-Electronic Records, Signatures - Compliance for Computer Systems Regulated by FDA
Carolyn Troiano
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices
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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