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The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) will be hosting a conference on June 9 on how to file an abridged marketing authorization application. Topics to be discussed will include: ● how to compile “a perfect dossier” ● how to prepare draft responses ● scientific advice meetings and their benefits, and ● the agency’s new “fee calculator.”
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INTERNATIONAL PHARMACEUTICAL QUALITY
Inside the Global Regulatory Dialogue
