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In review: the life sciences regulatory regime in United Kingdom

Published: February 23, 2022

This article reviews the essential regulatory considerations surrounding medicines and medical devices in United Kingdom, including clinical trials and marketing authorisations.

Source: lexology.com

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United KingdomNorthern IrelandGreat BritainAssociation Of The British Pharmaceutical IndustryUn Convention On Psychotropic SubstancesOrganisation For EconomicUn Single Convention On Narcotic DrugsEuropean CommissionPrescription Medicines Code Of Practice AuthorityAssociation Of British Healthcare IndustriesEuropean Federation Of Pharmaceutical IndustriesNational Health ServiceHome OfficeProperty OfficeEnforcement DivisionEuropean UnionGood Laboratory Practice RegulationsComplaints Adjudication PanelBorderline SectionScientific ProceduresEconomic Co OperationHuman UseClinical TrialsClinical Trial RegulationsEuropean Economic Area