EU-HTA: G-BA coordinates parallel scientific consultations for manufacturers from September

Federal Joint Committee (G-BA)

3 July 2023 - From 2025, a systematic evaluation of clinical studies for new medicinal products and medical devices will be carried out at European level in so-called EU-HTA reports (Joint Clinical Assessments) within the framework of the EU-HTA regulation. 

The European consultations (Joint Scientific Consultations) will also start in 2025, which will enable an early exchange between manufacturers, EMA and HTA organisations in Europe.

Read G-BA press release [German]

Michael Wonder

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Michael Wonder