The Need to Streamline Adverse Event Reporting for Clinical Trials

The Need to Streamline Adverse Event Reporting for Clinical Trials

News
11/12/18

Dr Andrew Rut, MyMeds&Me, explores in the Journal for Clinical Studies how consistent, high quality standardised and complete data is a foundation of successful clinical trials and drug development.

Read more here: http://www.jforcs.com/need-str...


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