Glossary of MHRA terms - D

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Click on a different letter in the list above for terms beginning with that letter.

D

DB
Device Bulletin. This is an MHRA devices publication.

DCP
DeCentralised Procedure. This is applicable in cases where an authorisation does not yet exist in any of the EU Member States.

DDX
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.

DH
DoH
Department of Health.

DHSSPSNI
Northern Ireland Department of Health, Social Services, and Public Safety

DMF
Drug Master File. This describes the active substance manufacturing process [See also: ASM].

DMRC
Defective Medicines Report Centre. This Unit assesses suspected quality defect reports and co-ordinates product recalls.

DR
Digital radiology.

DSU
Drug Safety Update.

DTS
Device Technology and Safety. 

 

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Page last modified: 23 September 2008