EU Pilots Real-Time Generation Of Electronic Product Information By Drug Companies

The pilot will for the first time use “real EU regulatory procedures” to test the creation and publication of electronic product information.

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ePI can make accessing accurate and up-to-date product information more convenient • Source: Shutterstock

The European Medicines Agency has announced plans to test the use of electronic product information (ePI) in regulatory procedures in a one-year pilot that will start in July.

The pilot, which will also involve drug regulators in Denmark, the Netherlands, Spain and Sweden, is key to furthering the EU ePI project, under which drug companies will be allowed to distribute information about their products (eg, summary of product characteristics, labeling and package leaflets) to

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