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EMA Mid-Year Report 2026: Reform, Supply and the First Joint Clinical Assessment

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By João L. Carapinha

November 4, 2026

Europe
Painted European harbour scene with a couple walking a dog past moored rowing boats

The EMA mid-year report 2026 (reference EMA/206392/2026, dated 29 October 2026) shows how the European Medicines Agency is delivering on its expanding remit. It covers the first half of 2026 and tracks progress in the main focus areas of the Single Programming Document (SPD) 2026-2028.

Legislation and supply: the new pharmaceutical law and the Critical Medicines Act

The provisional political agreement on the new pharmaceutical legislation (NPL) was reached on 11 December 2025 by the European Commission, the European Parliament and the Council. The report describes it as the most important overhaul of the regulatory framework in over two decades, changing how medicines are developed, authorised and made available to patients across the EU.

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