SignupTraining - Compliance, Certifications & technology Courses

Showing 31-40 of 704 items.

Webinar

View Details

Risk Assessment in Medical Device Design

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...

Webinar

View Details

4-Hour Virtual Training: How to Respond to an FDA Investigation

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. ...

Webinar

View Details

3-hr Virtual Seminar: Understanding Requirements of a Bioanalytical Method Validation

Gwendolyn Wise-Blackman

Recorded Duration : 180 Minutes

Life Sciences > Pharmaceutical | Biotchnology | Laboratory

Gwen Wise-Blackman has 20 years of combined experience in Cell-Based Assays and Quality Systems. She has worked at DuPont Pharmaceuticals, Catalent Pharma Solutions (formerly ...

Webinar

View Details

Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

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

Webinar

View Details

Medical Device Non-Product Software Validation Training

John E. Lincoln

Recorded Duration : 90 Minutes

Life Sciences > Medical Devices

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...

Webinar

View Details

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...

Webinar

View Details

Clinical Process Improvement

Joy L. McElroy

Recorded Duration : 90 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

Webinar

View Details

Steam Sterilization Microbiology and Autoclave Performance Qualification

Danielle DeLucy

Recorded Duration : 60 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...

Webinar

View Details

Problem Solving - Root Cause Analysis in Pharma Manufacturing

Joy L. McElroy

Recorded Duration : 75 Minutes

Life Sciences > Pharmaceutical

Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. ...

Webinar

View Details

Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configura...

Jose Mora

Recorded Duration : 90 Minutes

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

Jose Mora, is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences ind...

Your Search Result For All Webinars

Live Upcoming

Recorded

Understanding and Implementing a Technology Transfer Process

Steven Laurenz

LIVE : September 23 , 2025 01:00 PM EDT

GMPs for Medical Devices and Key Medical Device Observations

Charles H. Paul

LIVE : September 24 , 2025 01:00 PM EDT

Risk Assessment in Medical Device Design

Charles H. Paul

Recorded Duration : 60 Minutes

4-Hour Virtual Training: How to Respond to an FDA Investigation

Joy L. McElroy

Recorded Duration : 240 Minutes

3-hr Virtual Seminar: Understanding Requirements of a Bioanalytical Method Validation

Gwendolyn Wise-Blackman

Recorded Duration : 180 Minutes

Human Factors-Usability Based on ISO 62366

Recorded Duration : 60 Minutes

Medical Device Non-Product Software Validation Training

John E. Lincoln

Recorded Duration : 90 Minutes

Software Verification and Validation Planning and Documentation

John E. Lincoln

Recorded Duration : 90 Minutes

Clinical Process Improvement

Joy L. McElroy

Recorded Duration : 90 Minutes

Steam Sterilization Microbiology and Autoclave Performance Qualification

Danielle DeLucy

Recorded Duration : 60 Minutes

Problem Solving - Root Cause Analysis in Pharma Manufacturing

Joy L. McElroy

Recorded Duration : 75 Minutes

Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configura...

Jose Mora

Recorded Duration : 90 Minutes

hello