regulatoryRole

27 triples
GPTKB property

Random triples
Subject Object
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency ensuring medicines and medical devices work and are acceptably safe
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency post-market surveillance
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency monitoring of product safety
gptkb:CIMA_(Cayman_Islands) enforcement of financial laws
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency enforcing regulations
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency public health protection
gptkb:GAL3 positive regulator
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency recall of unsafe products
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency medical device registration
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency inspection and enforcement
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency inspecting manufacturers and distributors
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency pharmacovigilance
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency medical device safety
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency adverse event reporting
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency public health protection
gptkb:CIMA_(Cayman_Islands) market conduct supervision
gptkb:CIMA_(Cayman_Islands) prudential supervision
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency clinical trial authorisation
gptkb:Medicines_and_Healthcare_products_Regulatory_Agency licensing medicines
gptkb:UK_Medicines_and_Healthcare_products_Regulatory_Agency clinical trial approval

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