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RAC Pharmaceuticals EU Regulations Questions and Answers

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RAC Pharmaceuticals EU Regulations Questions and Answers ADR - ANSAdverse Drug Reaction AESGP - ANSAssociation of the European Self-medication Industry AIFA - ANSItalian Medicines Agency ATMP - ANSAdvanced Therapy Medicinal Products CA - ANSCompetent Authority CAT - ANSCommittee on Advanced Therapies CD-P-PH/ PHO - ANSEuropean Committee on Pharmaceuticals and Pharmaceutical Care CEN - ANSEuropean Committee for Standardization CHMP - ANSCommittee for Medicinal Products for Human Use CMD(h) - ANSCoordination Group for Mutual Recognition and Decentralised Procedures for human medicines CMS - ANSConcerned Member State COMP - ANSCommittee on Orphan Medicinal Products CP - ANSCentralized Procedure CTA - ANSClinical Trial Application CTD - ANSCommon Technical Document CTFG - ANSClinical Trials Facilitation Group CVMP - ANSCommittee for Veterinary Medicinal Products DAR - ANSDraft Assessment Report DCP - ANSDecentralized Procedure DG - ANSDirectorate Generals DLP - ANSData Lock Point DSUR - ANSDevelopment Safety

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Uploaded on
December 15, 2023
Number of pages
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Written in
2023/2024
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Questions & answers

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  • rac pharmaceuticals eu regulations questions and
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