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EU CLINICAL TRIAL AUTHORIZATIONS

Donawa Lifescience Consulting (DLC) is a full service European CRO, experienced in ethics committee submissions as well as clinical trial applications to national authorities. We can help meet site-specific ethics committee requirements, as well as national clinical study regulations and documentation requests.

The DLC Director of Clinical Affairs has many years’ experience in the management of drug clinical trials in Europe and beyond. Her team can provide full support to sponsors, including multi-site, multi-country management and monitoring.

For more information on our services for European drug clinical trials, visit our dedicated CRO website, or contact us by e-mail.