Compliance with The European Medicines Agency reflection paper on e-source data

(www.complianceonline.com)

The European Medicines Agency (EMA) has adopted a reflection paper on GCP inspectors’ expectations for e-source data (EMA/INS/GCP/454280/2010). The paper, which came into effect on 1 August 2010, outlines the current opinion of the EU GCP Inspectors Working Group on the use of electronic data capture in clinical trials and on related inspections.

This webinar will help you understand the compliance requirements concerning EMA reflection paper on e-source data (EMA/INS/GCP/454280/2010).

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