Version: 1.0.5 | Published: 21 Jun 2024 | Updated: 531 days ago
Dictionary of Medicines and Devices
Dataset
Summary
Type:
Information standards
Applies To:
- Health and Care Organisations purchasing systems that support recording and communication of information about medicines
- Health and Care Organisations using medicines\u0027 information for reimbursement, pharmacovigilance, drug utilisation, supply chain
Impacts On:
Suppliers of IT systems that support recording and communication of information
about medicines used in patient care including, but not limited to:
e-prescribing, administration, dispensing, medication history, reimbursement. No
changes are required to those electronic systems already using dm+d. No changes
are made to the distribution of data files. Pharmaceutical companies: no changes
need to be made by pharmaceutical companies supplying product details for use in
dm+d. No changes to the submission process are introduced.
Conformance Date:
30 June 2017
Topics:
- Clinical decision support
- Data definitions and terminologies
- Dispensing
- Messaging
- Prescribing
- Reference data
- Tests and diagnostics
Care Settings:
- Community health
- Hospital
- Maternity
- Mental health
- Pharmacy
- Urgent and Emergency Care
Alternate Name:
- DM+D
- Dictionary of Medicines and Devices (dm+d): Conversion
Documentation
Description:
This standard comprises:
- A model of the components required to represent a medicine used in patient care, along with additional components specific to the reimbursement process used in primary care.
- Content that is maintained and distributed according to approved policies and processes.
- A governance structure that supports requirements for an evolving but stable set of implementable terminology products.
- Identification of medicines within the supply chain by the inclusion of GS1 GTIN codes where known.
The scope of the standard in terms of content is for medicines only; medical devices are currently excluded. The primary purpose is to support interoperability. Therefore electronic systems that exchange or share information about medicines relating directly to a patient’s care must adhere to the standard by using dm+d identifiers and descriptions when transferring information.
Relations:
- Automatic Identification and Data CaptureDAPB0108
- Electronic Yellow Card ReportingDCB1582
- Clinical Risk Management: its Application in the Deployment and Use of Health IT SystemsDCB0160
- Clinical Risk Management: its Application in the Manufacture of Health IT SystemsDCB0129
- Read Clinical Terms Version 3ISB 1552
- Read Clinical Terms Version 2ISB 1553 SNOMED CT supersedes READ codes as a terminology.
- SNOMED CTSCCI0034
- Systemic Anti-Cancer Therapy Data SetDCB1533
- The Medical Dictionary for Regulatory Activities (MedDRA)
- HIV and AIDS Reporting System (HARS)SCCI1570
Document Control
Sponsor:
Elizabeth Woodeson, Department of Health
Approval Date:
28 March 2017
Business Lead:
Stuart Abbott, NHS Digital
Post Implementation Review Date:
30 June 2018
Scope:
NHS Services
SRO:
Alistair McDonald, NHS Business Services Authority
Technical Committee:
Standardisation Committee for Care Information (SCCI)
Mandated:
Yes
Status:
active
Legal Authorities
Legal Authority:
Section 250 of the Health and Social Care Act 2012
Legal Authority Description:
This information standard is published under section 250 of the Health and
Social Care Act 2012
Origin
Name:
NHSE-SD Data Catalogue