SignupTraining - Compliance, Certifications & technology Courses

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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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Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

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

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HVAC and GMP Environmental Control for Pharmaceutical Cleanrooms

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical

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Review of Chemistry, Manufacturing and Controls (CMC) of an Investigational New Drug Application (IN...

Recorded Duration : 60 Minutes

Life Sciences > Pharmaceutical | Biotechnology | Clinical | Laboratory

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Introduction to FDA and EU Medical Device Submissions

Charles H. Paul

Recorded Duration : 60 Minutes

Life Sciences > Medical Devices

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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How to Prepare For and Host a FDA Inspection and Respond to 483’s

Edwin Waldbusser

Recorded Duration : 60 Minutes

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 ...

Webinar

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Essentials of Validation – IQ, OQ, PQ

Recorded Duration : 90 Minutes

Life Sciences > Medical Devices

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Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Joy L. McElroy

Recorded Duration : 75 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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Recorded

6-hr Virtual Seminar: Quality Control Laboratory Compliance - cGMPs and GLPs

Joy L. McElroy

LIVE : May 06 , 2026 11:00 AM EST

FDA Audit Best Practices - Dos and Don'ts

Charles H. Paul

LIVE : May 06 , 2026 01:00 PM EST

Aseptic Processing & Aseptic Techniques

Carl Patterson, MS, SSGB, SSBB

LIVE : May 12 , 2026 01:00 PM EST

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

Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

HVAC and GMP Environmental Control for Pharmaceutical Cleanrooms

Recorded Duration : 60 Minutes

Review of Chemistry, Manufacturing and Controls (CMC) of an Investigational New Drug Application (IN...

Recorded Duration : 60 Minutes

Introduction to FDA and EU Medical Device Submissions

Charles H. Paul

Recorded Duration : 60 Minutes

How to Prepare For and Host a FDA Inspection and Respond to 483’s

Edwin Waldbusser

Recorded Duration : 60 Minutes

Essentials of Validation – IQ, OQ, PQ

Recorded Duration : 90 Minutes

Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing

Joy L. McElroy

Recorded Duration : 75 Minutes

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