CRN provide full support for clinical trial submission to regulatory authorities and ethics committees. We know the fast collection of essential sites documents and contracts execution is important for a fast submission and a short study start-up timelines.

CRN perform GCP trainings on-ongoing basis for the site study teams keeping GCP certificates updated as part of quality system.

We provide to any third party GCP training services with highly qualified trainers with more than 20 years in the clinical research industry.

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