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Chris
Bamford, PhD
Director, Regulatory Affairs, Regulatory and Start Up, Site Management

Chris is a Director in the Regulatory Affairs group within the QuintilesIMS Regulatory Start-Up organisation. In this role Chris is responsible for providing QuintilesIMS’ sponsors with advice in the conduct of clinical trial applications, amendments and general regulatory support relating to clinical trials.

He has worked within the Regulatory team at QuintilesIMS supporting sponsors for the past 8 years, and is also a member of an Expert Working Group and the Sponsor Stakeholder Group supporting the EMA in the development of the EU Portal and Database which will be a critical part of the forthcoming EU Regulation. Chris is also a member of the Association of CROs EU Scientific and Regulatory Committee.

Chris Bamford

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