Recording Adverse Events & Generating Quality Data

When Jan 15, 2016 from 12:30 PM to 01:30 PM
Where Edinburgh
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The process of safety reporting is well defined for CTIMPS, but recording adverse events is one of the most challenging areas of data entry. This seminar is designed to provide guidelines and practical insight of the does and dont’s of recording adverse events in CTIMPs and Non-CTIMPs.  

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