The European Commission on Thursday finalized rules on how it pools expertise from across the EU to assess the effectiveness of new drugs when compared to drugs already on the market. The rules are part of a broader initiative to bolster collaboration across the continent for evaluating and paying for new products.
Under the current framework, new health technologies undergo national-level assessments to determine their cost-effectiveness, which can be expensive and time-consuming. The new rules set timelines and concrete steps that member countries should follow when conducting joint assessments.
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