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EMA and HMA open big data regulatory documents to public consultation  1 Nov 2022

 

 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 here.

 

 

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