Submission – Registration authority and Ethics comittee
In the preparation of documentation, the completion and submission of the registration authority and the ethics committee adhere to all the rules that lead to the minimization of delays in approval due to low quality documentation. Based on contact with individual ethics committees we are able to recommend the best multicentre ethics committee with regard to the speed and quality of your requests discussion and subsequent exposure to the approval documents.
The same applies to other registration-related activities led clinical trial (additions, periodic reports, etc.)
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