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Full Service

Our intelligent clinical methods aid the drug development process for our sponsors in the following areas:

Our added value comes from our vast knowledge of specific local regulatory requirements, individual site and investigator relationships and logistical requirements in each of the countries we operate in.

QED is able to draw on the specific experience of its clinical teams in individual countries to leverage their relationships with Key Opinion Leaders, Investigators and sites within their regions.

Importantly this ensures a high response rate to feasibility assessments and capture of important country specific information via established local relationships and understanding of respective clinical trial environments.  This process is centrally coordinated to ensure a comprehensive feasibility assessment and site identification strategy can be provided, as required.

So whatever your requirement, from Clinical Monitoring to Logistical planning, you’ll find the essential elements are always supplied by QED.