Janet C. Donnelly BA, CIP, RAC
Practice Management
Silver Spring, Maryland, United States of America
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Ms. Donnelly will provide an overview of the good clinical practice program through a discussion of achievements in the regulation of FDA regulated clinical trials, the challenges facing Clinical Investigators, Sponsors, and IRBs in clinical research, and the various initiatives underway within FDA.
EVENTS & ACTIVITIES (Speaking, Spoken, and Authored)
FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference (Nov, 2016)
In-Person Event
Research and Clinical Research
Nov 03 - 04, 2016
New Orleans, Louisiana, USA
FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference (May, 2016)
- In-Person Event
- Research and Clinical Research
- May 11 - 12, 2016
- Philadelphia, Pennsylvania, USA
FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference (Nov, 2015)
- In-Person Event
- Research and Clinical Research
- Nov 04 - 05, 2015
- Boston, Massachusetts, USA
FDA Clinical Trial Requirements Regulations, Compliance and GCP Conference
- In-Person Event
- Research and Clinical Research
- Nov 05 - 06, 2014
- Lake Buena Vista, Florida, USA
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