All Clinical Trials starting in the European Union have to comply with CTIS Regulation and be conveyed through the Clinical Trial Information System (CTIS) as the common portal, aimed at homogenizing and standardizing the process across the EU.
ASPHALION has been part of the EMA CTIS stakeholder meetings and is also a CTIS Master Trainer, thus we are closely involved in the implementation of the Clinical Trial Regulation (CTR) and Clinical Trial Information System (CTIS).
Check out all the services packages we offer and how Asphalion can help your project: https://www.asphalion.com/ctis-training-and-tailored-consultancy/
For further information you can contact us at: [email protected]
