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Regulatory Services

QED appreciates the significance of high quality submissions to the relevant Regulatory Authorities and Ethics Committees to ensure that approvals are made in a timely fashion. We understand the complexities and the varying requirements of dealing with the numerous regulatory authorities and ethics committees around the world.

We have experts on the ground in each country which ensures that we have up-to-date local knowledge of the submission process, specific to the country.

In many cases our Senior CRAs will undertake the Ethics Committee submissions to ensure that the process is seamless from gaining approval to study start-up. Our team members have a thorough practical knowledge of completing Clinical Trial Applications.

Our teams have successfully completed submissions in some of the most challenging regulatory environments and so have a comprehensive understanding of the intricacies of each process and are able to communicate effectively with the relevant agencies and bodies.

Here are some of the areas QED can assist with:

Wherever you need to gain approval for your study globally: QED can help you achieve this.