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Risk Based Approaches for Clinical Trials
LIVE : August 02 , 2024 01:00 PM EDT
Life Sciences > Clinical | Biotechnology | Laboratory
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Clinical Process Improvement
Joy L. McElroy
LIVE : August 07 , 2024 01:00 PM EDT
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. ...

Showing 11-20 of 27 items.
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Clinical Trial Master File Compliance
Carolyn Troiano
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory
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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Risk-Based Quality and Compliance Management in Clinical Trials with Combination Products
Marina Malikova
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dr. Malikova has over twenty years of experience in the clinical research field. She has managed Phase I – IV studies involving investiga...

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Trial Master File: Designing, Operationalizing and Maintaining a Comprehensive Assessment
Marina Malikova
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dr. Malikova has over twenty years of experience in the clinical research field. She has managed Phase I – IV studies involving investiga...

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Intelligent Approach to Risk-Based Monitoring to Improve Clinical Trial Quality
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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CRO Oversight: Practicalities, Roles and Responsibilities Discussion
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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Clinical QMS Compliance
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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Trial Master File (TMF): FDA Expectations From Sponsors and Sites
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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Writing Effective SOPs for FDA and CLIA Regulated Companies
Angela Bazigos
Recorded Duration : 90 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory
Angela Bazigos, is the CEO of Touchstone Technologies, Inc. She has 40 years of experience working in hospitals and Pharma industry. Her background includes companies like Roc...
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Ensuring Compliance Of Your Bioanalytical Method Validation With The 2013 FDA Draft Guidance
Brian Kirk
Recorded Duration : 75 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory
Brian A. Kirk, Ph.D. has been employed in both the biotech and pharmaceutical industries for over 20 years. He has a wealth of experience, working in the areas of synthetic or...
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Federal Oversight of Laboratory-Developed Tests: Where FDA & Congress Is Heading in 2018
Dennis Weissman
Recorded Duration : 60 Minutes
Life Sciences > Clinical | Biotechnology | Laboratory

Dennis Weissman, A nationally recognized, independent analyst and thought leader in the diagnostic field for over three decades, Dennis is Pres...

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