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![[Dividing Line Image]](../../images/div.gif)
Clinical Trial Supervision
and Consultation
- Patient Eligibility
- Adverse Event Review and Reporting
- Assessment of Scientific Data
- Study Design
- Clinical Review of Documents
- Client Representation at Governmental Agency Meetings
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Send mail to Michael Gendron, Ph.D.
with questions
or comments about this web site.
Copyright © 1997-2000 Precision Research, Inc.
Last modified: November 28, 2000
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