Non CTIMP – Serious Adverse Event Report Form V6

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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
02.02.2022
Date Review
04.01.2025
File Size
112Kb