ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit-CRU The RSA must be informed of adverse events to assess if the risk: benefit status of the study has changed. In general, an Adverse Event (AE) is any untowa - Status effect - Document - PDFSEARCH.IO

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	ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit-CRU The RSA must be informed of adverse events to assess if the risk: benefit status of the study has changed. In general, an Adverse Event (AE) is any untowa Add to Reading List Document Date: 2014-10-31 14:07:24 Open Document File Size: 22,96 KB Share Result on Facebook Company Possibly Related AE / Serious AE / Other Unexpected AE / / MedicalCondition hypertension / GERD / severe GERD / / Organization ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit / / Position investigator / current Investigator / / Technology research protocol / / SocialTag Pharmaceutical sciences Pharmaceutics Adverse event Serious adverse event Clinical trial Randomized controlled trial Risk Clinical research coordinator Adverse effect Clinical research

ADVERSE EVENT REPORTING GUIDELINES CCF Clinical Research Unit-CRU The RSA must be informed of adverse events to assess if the risk: benefit status of the study has changed. In general, an Adverse Event (AE) is any untowaAdd to Reading List