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EMA opens the early dialogue to the development of anti-infective therapeutics

EMA’s vision on evidence by design to evaluate the added therapeutic...

The EURIPID Collaboration for pricing and reimbursement

EMA’s first guideline on medical devices integral to medicinal products

Consultation on the future of Regulatory Sciences to 2025

New Q&As on safety features from the EU Commission

EMA opened a consultation on the use of patient registries for...

The use of real world data for R&D of pharmaceuticals

Brexit: EU Commission warns on possible issues regarding clinical trials

Regulators launched activities to prepare for the Brexit

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