Printed 25/05/2013

Url http://www.dkma.dk/en/topics/side-effects-and-trials/clinical-trials/news/reflection-paper-from-emeas-gcp-inspecto--al-trials-

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Reflection paper from EMEA's GCP Inspectors Working Group on expectations for electronic source documents used in clinical trials

The EMEA GCP Inspectors Working Group has prepared a reflection paper on the handling of electronic documents in connection with clinical trials.

You can download the document in the factbox to the right.

The Danish Medicines Agency, 11 January 2008

Created 11 January 2008

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Danish Health and Medicines Authority
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