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Do it right the first time!
This is the credo of the Accovion experienced clinical trial submission team. The team provides regulatory compliant quality application dossiers for the conduct of a clinical trial to be submitted to the competent authorities and the applicable ethics committees. The team is dedicated to ensuring the completeness and accuracy of your submitted information and of the necessary supportive documentation for the demonstration of quality, safety and efficacy of your investigational medicinal product or medical device and the conduct of your planned trial.
Of course, we can also assist you with any amendments to your trial as well as inform all necessary parties about the end of the clinical trial.
The Accovion team supports you with negotiations and answering questions from competent authorities and ethics committees concerning your clinical trial project.
Dr. Rainer Porrmann
Manager Study Coordination & Clinical Trial Submission
+49 6196 7709-385
