|Articles|May 1, 2002
- Applied Clinical Trials-05-01-2002
Identifying and Documenting Adverse Events at Clinical Study Sites
Improving adverse event reporting can lead to improved safety profiles and, consequently, fewer drugs pulled from the market.
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Articles in this issue
almost 24 years ago
Letters to the Editoralmost 24 years ago
Parents for Orphansalmost 24 years ago
Fraud, Abuse, and Consentalmost 24 years ago
Brian Koziolalmost 24 years ago
A Model-Based Method for Improving Protocol QualityNewsletter
Stay current in clinical research with Applied Clinical Trials, providing expert insights, regulatory updates, and practical strategies for successful clinical trial design and execution.
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