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How to Handle the Most Common Problems Related to FDA Software Validation and Verification

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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How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

Jeff Kasoff

Recorded Duration : 60 Minutes

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...

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3-hr Virtual Seminar: Technical Writing for the Pharmaceutical, Medical Device and Biotech Industrie...

Joy L. McElroy

Recorded Duration : 180 Minutes

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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The Most Common Problems in FDA Software Validation & Verification

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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Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Webinar

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4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance

Carolyn Troiano

Recorded Duration : 240 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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FDA Audit Best Practices - Dos and Don'ts

Charles H. Paul

Recorded Duration : 60 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

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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Write it Right – Well Written Procedures are Essential for QMS Effectiveness

Joy L. McElroy

Recorded Duration : 60 Minutes

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. ...

Webinar

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Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

Life Sciences > Medical Device | Diagnostic | Pharmaceutical | Biologics fields

Webinar

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Software Verification and Validation Planning and Documentation

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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The Human Error Tool Box: A Practical Approach to Human Error

Dr. Ginette Collazo

LIVE : September 03 , 2025 01:00 PM EDT

How to Handle the Most Common Problems Related to FDA Software Validation and Verification

Carolyn Troiano

Recorded Duration : 90 Minutes

How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

Jeff Kasoff

Recorded Duration : 60 Minutes

3-hr Virtual Seminar: Technical Writing for the Pharmaceutical, Medical Device and Biotech Industrie...

Joy L. McElroy

Recorded Duration : 180 Minutes

The Most Common Problems in FDA Software Validation & Verification

John E. Lincoln

Recorded Duration : 90 Minutes

Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance

Carolyn Troiano

Recorded Duration : 240 Minutes

FDA Audit Best Practices - Dos and Don'ts

Charles H. Paul

Recorded Duration : 60 Minutes

Write it Right – Well Written Procedures are Essential for QMS Effectiveness

Joy L. McElroy

Recorded Duration : 60 Minutes

Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

Software Verification and Validation Planning and Documentation

John E. Lincoln

Recorded Duration : 90 Minutes

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