Click on a different letter in the list above for terms beginning with that letter.
Device Bulletin. This is an MHRA devices publication.
DeCentralised Procedure. This is applicable in cases where an authorisation does not yet exist in any of the EU Member States.
Doctors and Dentist Exemptions. These are letters of approval issued by the Clinical Trials Section to doctors and dentists who want to do drug research.
Department of Health.
Northern Ireland Department of Health, Social Services, and Public Safety
Drug Master File. This describes the active substance manufacturing process [See also: ASM].
Defective Medicines Report Centre. This Unit assesses suspected quality defect reports and co-ordinates product recalls.
Drug Safety Update.
Device Technology and Safety.