Clinical Trials
The new EU Clinical Trials Regulation (Regulation No. 536/2014) will come into force in 2019. The regulation aims at streamlining and simplifying rules in order to revive research activity in Europe, for example by introducing a unified application process through a single EU portal for cross-border trials.
Simplification of rules include:
- Streamlined application procedure via a single entry point – an EU portal and database, for all clinical trials conducted in Europe;
- Single authorisation procedure for all clinical trials, with assessment of application by all Member States concerned, with one single assessment outcome and authorisation per Member State;
- Extension of the tacit agreement principle to the whole authorisation process for more legal certainty for sponsors, researchers, SMEs and academics;
- Strengthened transparency for clinical trials data and new rules for informed consent for use of subjects’ data
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