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EMA and HMA open big data regulatory documents to public consultation 

EMA and HMA open big data regulatory documents to public consultation 

The European Medicines Agency and the Heads of Medicines Agencies in the EU Member States are advancing their agenda to improve data quality for medicine regulation decision-making, publishing the draft Data Quality Framework and a draft good practice guide for the use of the EU metadata catalogue of real-world data sources for consultation this month. Read more.

1 Nov 2022
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