Non CTIMP – Serious Adverse Event Report Form V 1

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Overview
For use when reporting  a Non CTIMP Serious Adverse Event report use in conjunction with SOP 206  Adverse Events: Identifying Recording and Reporting adverse events for Non-CTIMP Healthcare Research Studies Trust Docs number 14932
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Reference
Date Uploaded
03.06.2020
Date Review
27.05.2023
File Size
114Kb