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Choose QED for the conduct of your study in North America

North America Western Europe Central & Eastern Europe South America Russia, Ukraine & Baltic States Asia Pacific India Middle East Africa

The US is world-renowned for excellent standards of care, extremely high levels of training and expertise in specialist and critical healthcare with unsurpassed investment in clinical research.

Each clinical trial in the U.S. has to be approved and monitored by an Institutional Review Board (IRB) to ensure that any risks are minimised and would justify the potential benefits. An IRB consists of an independent group of physicians, statisticians, community advocates, and other parties who guarantee that a clinical trial is ethical and protects the rights of the study participants. Ultimately, each application is subject to review and approval by the US Food and Drug Administration (FDA).

QED can help you realise the following advantages to conducting your clinical trial in North America:

QED has the knowledge and expertise to successfully deliver studies across North America.