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Showing 21-27 of 27 items.

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General Data Protection Regulation (GDPR): Compliance for Clinical Trials

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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The Secret of Study Conduct Documentation to ensure a successful Audit: What the FDA Inspectors look...

Dr. Charles H Pierce

Recorded Duration : 90 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Charles H Pierce is Medical Director of Pierce One Consulting. From an original Master’s thesis (Pharmacology) in 1961 (Minnesota) throug...

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The Sunshine Act: Reporting for Clinical Trials

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for huma...

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Adverse Event Reporting Understanding Regulatory Reporting Requirements

Nicole Tesar

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Nicole began her career in Clinical Research over 17 years ago as a Clinical Research Associate for a small Clinical Research Organization. The...

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Protocol Deviations: Documenting, Managing, and Reporting

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for huma...

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Investigational Product Accountability Best Practices

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for huma...

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Analyzing Assay Validation for Clinical Diagnostics

Todd Graham

Recorded Duration : 60 Minutes

Life Sciences > Clinical | Biotechnology | Laboratory

Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for ...

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Risk Based Approaches for Clinical Trials

LIVE : August 02 , 2024 01:00 PM EDT

Clinical Process Improvement

Joy L. McElroy

LIVE : August 07 , 2024 01:00 PM EDT

General Data Protection Regulation (GDPR): Compliance for Clinical Trials

Dr. Laura Brown

Recorded Duration : 60 Minutes

The Secret of Study Conduct Documentation to ensure a successful Audit: What the FDA Inspectors look...

Dr. Charles H Pierce

Recorded Duration : 90 Minutes

The Sunshine Act: Reporting for Clinical Trials

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Adverse Event Reporting Understanding Regulatory Reporting Requirements

Nicole Tesar

Recorded Duration : 60 Minutes

Protocol Deviations: Documenting, Managing, and Reporting

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Investigational Product Accountability Best Practices

Sarah Fowler-Dixon

Recorded Duration : 60 Minutes

Analyzing Assay Validation for Clinical Diagnostics

Todd Graham

Recorded Duration : 60 Minutes

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