‘Quick Guide’ To Help EU Clinical Trial Sponsors As CTIS Hits 31 January Milestone

Just a day before it became mandatory to use the single-portal Clinical Trial Information System, the European Commission published concise advice for sponsors and investigators who want to conduct trials in Europe.

Young businessman thinks over the steps for successful growth: Clinical trial
The CTR is designed to streamline the processes for the application and supervision of clinical trials • Source: Shutterstock

With the EU’s single-portal Clinical Trial Information System (CTIS) becoming mandatory from 31 January for sponsors seeking trial approval, the European Commission has issued a “quick guide” to help companies and investigators understand how to implement the Clinical Trials Regulation (CTR).

The 27-page guide was published on 30 January, the day before the CTR hit the major milestone of the...

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