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HVAC and GMP Environmental Control for Pharmaceutical Cleanrooms
LIVE : August 12 , 2025 01:00 PM EDT
Life Sciences > Pharmaceutical
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3-hr Virtual Seminar: Technical Writing for the Pharmaceutical, Medical Device and Biotech Industrie...
Joy L. McElroy
LIVE : August 14 , 2025 01:00 PM EDT
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

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Writing and Enforcing Effective Standard Operating Procedures (SOP) and Work Instructions
Joy L. McElroy
LIVE : August 19 , 2025 01:00 PM EST
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

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How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Jeff Kasoff
LIVE : August 19 , 2025 01:00 PM EDT
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Jeff Kasoff, RAC, CMQ/OE, Lean Black Belt, has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operat...
Showing 551-560 of 702 items.
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Importance Of Environmental Monitoring In A Contamination Controlling Plan
Erika L. Roberts, M.F.S
Recorded Duration : 60 Minutes
Life Sciences > Pharma | Biotech | Medical Devices
Erika L. Roberts, M.F.S, is a Masters in Forensic Science (with an emphasis in document examination) and currently works as a Senior Quality Assurance Analyst and as a freelan...
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Why I Should Test Raw Materials for Microbial Presence and What Are The Microbiological and Business...
Henry Urbach
Recorded Duration : 90 Minutes
Life Sciences > Biotechnology
Henry Urbach is the founder of GMP Training, Development and Consulting. GMP TDC LLC is a New York-based consulting organization serving Life Sciences industries. Henry has 25...
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Understanding Vendor Verification and Monitoring Programs
Natasha Rowley-Phipps
Recorded Duration : 75 Minutes
Life Sciences > Food Safety And Dietary Supplements
Natasha Rowley-Phipps has had more than 18 years of experience in food quality, nutrition labeling, manufacturing and research. Natasha graduated from Kansas State University ...
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Professional Guidance on Conducting a Comprehensive HIPAA Risk Analysis
Roya Camille Keyan
Recorded Duration : 60 Minutes
Life Sciences > Healthcare | Clinical | Pharmaceuticals

Roya Camille Keyan established HR Advisory Group Ltd in 2005 to address the growing need for expert, accessible, outsourced regulatory complian...

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Effective FDA Complaint Handling and Product Recalls
Joy L. McElroy
Recorded Duration : 75 Minutes
Life Sciences > All FDA Regulated Industries

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

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Understanding The Regulation of Prescription Drugs
Dr. Loren Gelber
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotchnology | Laboratory
Dr. Loren Gelber has worked in the pharmaceutical industry for more than 40 years, at both the FDA and in private industry. She has been involved in numerous launches of OTC d...
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How to Conduct a Human Factors/ Usability 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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Clinical Trial Monitoring - Documentation and Closure
Sarah Fowler-Dixon
Recorded Duration : 90 Minutes
Life Sciences > Clinical Trial
Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for huma...
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Clinical Trial Monitoring - Documentation and Closure
Sarah Fowler-Dixon
Recorded Duration : 90 Minutes
Life Sciences > Clinical Trial
Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for huma...
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Federal Oversight of Laboratory-Developed Tests: Where FDA & Congress Is Heading in 2018
Dennis Weissman
Recorded Duration : 60 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dennis Weissman, A nationally recognized, independent analyst and thought leader in the diagnostic field for over three decades, Dennis is Pres...

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