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Virtual Site Audits for FDA Regulated Industries

John E. Lincoln

Recorded Duration : 90 Minutes

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...

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Effective Document Management for Pharma, Biotech & Medical Device

Joy L. McElroy

Recorded Duration : 90 Minutes

Life Sciences > Pharma | Biotech | Medical Devices

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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3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

Danielle DeLucy

Recorded Duration : 180 Minutes

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...

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Good Clinical Practices Review of ICH E6

Charles H. Paul

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles is a management consultant...

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Fundamentals of Toxicology for the Pharmaceutical Industry

Dr. Stefano Persiani

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Dr. Stefano Persiani is currently Director of Translational Sciences and Pharmacokinetics at Rottapharm Biotech, Italy. He graduated in Pharmac...

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Best Practices for Preparing for an FDA Inspection

Susanne Manz

Recorded Duration : 90 Minutes

Life Sciences > Medical Devices

Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background ...

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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 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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4-Hour Virtual Seminar on Analytical Instrument Qualification and Validation – Understanding Use o...

Joy L. McElroy

Recorded Duration : 240 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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Biomarkers in Drug Discovery and Development

Dr. Stefano Persiani

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

Dr. Stefano Persiani is currently Director of Translational Sciences and Pharmacokinetics at Rottapharm Biotech, Italy. He graduated in Pharmac...

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Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467>

Joy L. McElroy

Recorded Duration : 90 Minutes

Life Sciences > Pharmaceutical | Biotchnology | 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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Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Joy L. McElroy

LIVE : November 05 , 2025 01:00 PM EDT

Virtual Site Audits for FDA Regulated Industries

John E. Lincoln

Recorded Duration : 90 Minutes

Effective Document Management for Pharma, Biotech & Medical Device

Joy L. McElroy

Recorded Duration : 90 Minutes

3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations

Danielle DeLucy

Recorded Duration : 180 Minutes

Good Clinical Practices Review of ICH E6

Charles H. Paul

Recorded Duration : 60 Minutes

Fundamentals of Toxicology for the Pharmaceutical Industry

Dr. Stefano Persiani

Recorded Duration : 60 Minutes

Best Practices for Preparing for an FDA Inspection

Susanne Manz

Recorded Duration : 90 Minutes

21 CFR Part 11 (electronic records/signatures) Compliance for Computer Systems Regulated by FDA

Carolyn Troiano

Recorded Duration : 90 Minutes

4-Hour Virtual Seminar on Analytical Instrument Qualification and Validation – Understanding Use o...

Joy L. McElroy

Recorded Duration : 240 Minutes

Biomarkers in Drug Discovery and Development

Dr. Stefano Persiani

Recorded Duration : 60 Minutes

Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467>

Joy L. McElroy

Recorded Duration : 90 Minutes

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