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In review: the life sciences regulatory regime in Malta

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

United Kingdom , Roche Bolar , Veterinary Services , National Accreditation Body , Single Convention On Narcotic Drugs , Borderline Classification Committee , Department Of Health , Enforcement Directorate Of The Medicines Authority , Good Laboratory Practice Regulations , Malta Pharmacy Council , European Parliament , Council Of Health , European Patent Convention , Committee For Unlicensed Medicinal Products , European Council Regulation , Medicines Authority Borderline Classification Committee , Ministry For Health , Customs Authority , Advisory Committee , Licensing Directorate Of The Medicines Authority , Licensing Authority , Single Convention , Council For Animal Welfare , Exceptional Medicinal Treatment Committee , Medicines Authority , Committee Regulations ,

In review: the life sciences regulatory regime in United Kingdom

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

United Kingdom , Northern Ireland , Great Britain , Association Of The British Pharmaceutical Industry , Un Convention On Psychotropic Substances , Organisation For Economic , Un Single Convention On Narcotic Drugs , European Commission , Prescription Medicines Code Of Practice Authority , Association Of British Healthcare Industries , European Federation Of Pharmaceutical Industries , National Health Service , Home Office , Property Office , Enforcement Division , European Union , Good Laboratory Practice Regulations , Complaints Adjudication Panel , Borderline Section , Scientific Procedures , Economic Co Operation , Human Use , Clinical Trials , Clinical Trial Regulations , European Economic Area , United Kingdom Manufacturing ,

Exemptions from Devices regulations during the coronavirus (COVID-19) outbreak

How to get fast-track approval of medical devices during COVID-19. ....

United Kingdom , Northern Ireland , Great Britain , Department Of Health , Social Care , Protective Equipment , United Kingdom Responsible Person , Northern Ireland Based Authorised Representative , Medical Devices Regulations ,

Canada regulations news for medical devices and IVDs

MedTech industry news ....

Health Canada , Medical Device Regulations , Periodic Benefit Risk Evaluation Report , Medical Devices Regulations , Canada Gazette , Periodic Safety Update Report , Medical Devices ,

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