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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 391-400 of 705 items.
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CRO Oversight: Practicalities, Roles and Responsibilities Discussion
Dr. Laura Brown
Recorded Duration : 60 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dr. Laura Brown is an independent QA and Training Consultant and Director of the MSc in Clinical Research, School of Pharmacy at the University...

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How to Prepare for FDA Inspections and Customer Audits of Pharmaceuticals
Dr. Loren Gelber
Recorded Duration : 90 Minutes
Life Sciences > Pharma | Biotech | Medical Devices
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 Implement the ISO 13485 in Your Company?
Dr. Frank Stein
Recorded Duration : 90 Minutes
Life Sciences > Medical Devices

Prof. Dr. Dr. h.c. Frank Stein, medical engineer, medical engineering experience since 25 years, clinical and research experience in cardiac su...

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Sustainable Vendor Qualification in Pharma Industry
Gowri Sukumar
Recorded Duration : 60 Minutes
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Gowri Sukumar is the Director, CMC and Regulatory Affairs for Iterion Therapeutics, Houston, TX. Unique to her experience is leading all the te...

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Clinical QMS Compliance
Dr. Laura Brown
Recorded Duration : 60 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dr. Laura Brown is an independent QA and Training Consultant and Director of the MSc in Clinical Research, School of Pharmacy at the University...

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3-hr Virtual Seminar: Understanding GMP & cGMP Compliance - What it really means
Lynette N. Pious
Recorded Duration : 180 Minutes
Life Sciences > Pharmaceutical | Biotechnology | Clinical | 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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The Requirements and Responsibilities of a HIPAA Security | Privacy Officer
Howard Jones
Recorded Duration : 60 Minutes
Life Sciences > Healthcare

Howard Jones is keynote speaker at Compliance Key, Inc. He has been an independent consultant to physicians and hospitals since 1980. He has pr...

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Successfully Dealing with Out of Specification (OOS) Test results in the Pharmaceutical and Medical ...
Meena Chettiar
Recorded Duration : 60 Minutes
Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Ms. Chettiar received her M.S. in Regulatory Affairs for Medical Devices in Minnesota, USA, and M.A.SC in Chemical Engineering from University ...

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Medical Device Single Audit Program (MDSAP) - A New Face of Audit
Parul Chansoria, RAC
Recorded Duration : 60 Minutes
Life Sciences > Medical Devices
Parul is a Medical Device Professional with successful experience in initiation & implementation of Quality & Regulatory activities for different phases of a medical p...
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Compliance with the New ICH GCP Revision 2 Addendum
Dr. Laura Brown
Recorded Duration : 90 Minutes
Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Dr. Laura Brown is an independent QA and Training Consultant and Director of the MSc in Clinical Research, School of Pharmacy at the University...

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