EMA releases updated QRD Style Guide– say no to “drugs”
The European Medicines Agency (EMA) is responsible for evaluating, supervising, and monitoring medicines for safety– its mission is to foster scientific excellence in the assessment and management of medicines in the EU. Committed to providing clear and unbiased information, the EMA employs a variety of regulatory mechanisms that are continuously evaluated and optimized for the benefit of the public.
The EMA recently published its compilation of Quality Review of Documents (QRD) decisions about the stylistic guidelines in product information– citing frequent translation issues and providing additional policies that directly impact multilingual labeling and packaging.
