EN ISO 17523:2016
Current
The latest, up-to-date edition.
Health informatics - Requirements for electronic prescriptions (ISO 17523:2016)
29-06-2016
European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Conformance
5 General information
6 Requirements for electronic prescriptions
Annex A (normative) - Data elements
Annex B (informative) - Examples of elements and
implementations of electronic prescription
Bibliography
ISO 17523:2016 specifies the requirements that apply to electronic prescriptions. It describes generic principles that are considered important for all electronic prescriptions.ISO 17523:2016 is constrained to the content of the electronic prescription itself, the digital document which is issued by a prescribing healthcare professional and received by a dispensing healthcare professional. The prescribed medicinal product is to be dispensed through an authorized healthcare professional with the aim of being administered to a human patient. Other messages, roles and scenarios (e.g. validation of a prescription, administration, medication charts, EHR of the patient, reimbursement of care and dispensed products) are out of scope of this International Standard, because they are more or less country or region specific, due to differences in culture and in legislation of healthcare. However, requirements and content of electronic prescriptions within the context of jurisdictions have a relationship with these scenarios. The way in which electronic prescriptions are made available or exchanged also fall outside the scope of this International Standard.ISO 17523:2016 is applicable to electronic prescriptions of medicinal products. Although other kinds of products (e.g. medical devices, wound care products) can be ordered by means of an electronic prescription, the requirements in this International Standard are aimed at medicinal products that have a market authorization and at pharmaceutical preparations which are compounded in a pharmacy. An electronic prescription is an information object that authorizes a healthcare professional to legally dispense a medicinal product.ISO 17523:2016 specifies a list of data elements that can be considered as essential for electronic prescriptions, depending on jurisdiction or clinical setting (primary healthcare, hospital, etc.).
Committee |
CEN/TC 251
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Current
|
Standards | Relationship |
NF EN ISO 17523 : 2016 | Identical |
BS EN ISO 17523:2016 | Identical |
PN EN ISO 17523 : 2016 | Identical |
UNI EN ISO 17523 : 2016 | Identical |
NS EN ISO 17523 : 2016 | Identical |
I.S. EN ISO 17523:2016 | Identical |
UNE-EN ISO 17523:2016 | Identical |
DIN EN ISO 17523:2016-12 | Identical |
ISO 17523:2016 | Identical |
NEN EN ISO 17523 : 2016 | Identical |
DIN EN ISO 17523 E : 2016 | Identical |
SN EN ISO 17523:2016 | Identical |
PNE-prEN ISO 17523 | Identical |
ISO 17090-1:2013 | Health informatics Public key infrastructure Part 1: Overview of digital certificate services |
ISO/TS 27527:2010 | Health informatics Provider identification |
ISO 11615:2017 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information |
ISO/IEC 24760-1:2011 | Information technology Security techniques A framework for identity management Part 1: Terminology and concepts |
ISO 21549-7:2016 | Health informatics — Patient healthcard data — Part 7: Medication data |
ISO/TS 22220:2011 | Health informatics — Identification of subjects of health care |
ISO 11240:2012 | Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of units of measurement |
ISO 7498-2:1989 | Information processing systems Open Systems Interconnection Basic Reference Model Part 2: Security Architecture |
ISO 11238:2012 | Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of regulated information on substances |
ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
ISO 11616:2017 | Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information |
ISO 639-3:2007 | Codes for the representation of names of languages — Part 3: Alpha-3 code for comprehensive coverage of languages |
ISO 639-2:1998 | Codes for the representation of names of languages — Part 2: Alpha-3 code |
ISO/IEC 2382:2015 | Information technology — Vocabulary |
ISO 11239:2012 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.