trust in acromion
Following the full entry into force of CTR 536/2014 and the launch of the CTIS portal on 30 January 2022, we now have the desired harmonization of the submission process for (the vast majority of) clinical trials to be conducted in the EU. The application – via the CTIS portal – is exciting and requires a comprehensive knowledge of the individual modules.
acromion has many years of experience in dealing with regulatory databases, regardless of the type of clinical study, and remains your reliable partner.