You are in the planning phase of the approval of your medicinal products?
You need assistance in determining of a program of study and / or study protocol?
You need an experienced and competent partner in the implementation and conduct of your clinical trial?
Dr. Notghi Contract Research GmbH conducts clinical trials in compliance with scientific and ethical standards (ICH-GCP), in which, through regulations, e.g. of inclusion criteria for the patients and of the way of treatment, influence or interference factors are largely reduced.
We support you competently and reliably in all phases of clinical trials, from planning the study, to the implementation up to the successful completion of the study. Furthermore we have a wide network of experienced specialists available for subject-specific questions.
We gladly take on the communication with authorities, from filing through to completion of the study.
Our experts will gladly advice you personally. We look forward to your call or your message.