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Good Documentation Guideline (Chapter <1029> USP)
Dr. Afsaneh Motamed Khorasani
LIVE : October 16 , 2025 01:00 PM EDT
Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Dr. Afsaneh Motamed Khorasani, PhD, is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical sc...

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How to Prepare For and Host a FDA Inspection and Respond to 483’s
Edwin Waldbusser
LIVE : October 16 , 2025 01:00 PM EDT
Life Sciences > Medical Devices
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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2-hr Virtual Seminar: FDA Inspections - Understanding the Core Elements
LIVE : October 22 , 2025 01:00 PM EDT
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
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Essentials of Validation – IQ, OQ, PQ
LIVE : October 23 , 2025 01:00 PM EDT
Life Sciences > Medical Devices
Showing 581-590 of 702 items.
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HIPAA and The Administrative Subpoena: How to Protect Yourself from State Medical Licensure Boards a...
Mark Brengleman
Recorded Duration : 60 Minutes
Life Sciences > Healthcare
Mark worked as the assigned counsel to numerous health professions licensure boards as an Assistant Attorney General for the Commonwealth of Kentucky. Moving to private practi...
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Health Policy Changes & Trends in the Trump Era: Insurance and Market Outlook For 2018
Dennis Weissman
Recorded Duration : 75 Minutes
Life Sciences > Healthcare

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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FDA Regulatory Control of the Drug Development Process and Investigator Responsibility in the Proces...
Dr. Charles H Pierce
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Charles H Pierce is Medical Director of Pierce One Consulting. From an original Master’s thesis (Pharmacology) in 1961 (Minnesota) throug...

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Understanding GMP & cGMP Compliance
Lynette N. Pious
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotchnology | Laboratory
Lynette N. Pious is a quality systems and regulatory affairs consultant in the cosmetic, personal care and pharmaceutical industries. Lynette is the President and CEO of Pious...
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3 Hours Virtual Seminar: China Compliance Processes for Life Science Products: Company Establishment...
Robert J. Russell
Recorded Duration : 180 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bo...
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3-hr Virtual Seminar: Developing Documents and Records to Meet the Requirements of ISO,IEC 17025
Michael Brodsky
Recorded Duration : 180 Minutes
Life Sciences > Pharmaceutical | Biotchnology | 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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3 Hours Virtual Seminar: Latin America Understanding Regulatory Compliance Requirements Across the L...
Robert J. Russell
Recorded Duration : 180 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields
Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bo...
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3 Hours Virtual Seminar: What to Expect in A Federal HIPAA Audit & How to Avoid a Federal Audit
Brian Tuttle
Recorded Duration : 180 Minutes
Life Sciences > Healthcare
Brian Tuttle CPHIT, CHP, CBRA, Net+, A+, CCNA, MCP is a Certified Professional in Health IT (CPHIT), Certified HIPAA Professional (CHP), Certified Business Resilience Auditor ...
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Risk Based Clinical Trial Monitoring
Marie Dorat
Recorded Duration : 75 Minutes
Life Sciences > Clinical Trial
Marie Dorat, CQA,CAA is a QA/RA compliance, GxP Training and International product registration Consultant with 17 years  experience, in the Pharmaceutical/Medical Device...
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QSR-Compliant Equipment Control & Validation of Processes in the Manufacturing Environment
Joy L. McElroy
Recorded Duration : 90 Minutes
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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