EU Extends Pilot On Using Raw Data In Medicines Reviews ‘Until Further Notice’

EU regulators have recommended extending a pilot on the use of raw clinical trial data in medicines evaluations after an interim review of the initiative found that using such data improved regulatory decision-making.

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Current DCT digital platforms have limited functionality and technical capabilities • Source: Shutterstock

The European Medicines Agency and EU Heads of Medicines Agencies have published interim results from a proof-of-concept pilot investigating the benefits of using raw data from clinical trials in regulatory procedures.

In the 18 October report, the EMA and HMA said that a survey of pilot participants revealed the value of...

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