4 April 2017

CenterWatch: KCR Regulatory Expert’s View on EU CTR Implementation

KCR’s Anna Kubik, Director Regulatory Affairs, who was a speaker at the DIA EuroMeeting 2017, presented an overview of the current status focusing on the development of local requirements in terms of ethical assessment as well as proposed schemes respectively. Read our Regulatory Expert’s view on EU CTR Implementation at CenterWatch News, online publication with news and views on the clinical trial industry.

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