NEN-EN-ISO 21549-7:2004 Ontw. en

Medische informatica - Patiëntgezondheidskaart gegevens - Deel 7: Elektrionisch voorschrijven (medicatie data)

  • Deze norm is ingetrokken sinds 19-06-2007


Over deze norm

Status Ingetrokken
Aantal pagina's 34
Commissie Informatievoorziening in de zorg
Gepubliceerd op 01-10-2004
Taal Engels
This Draft International Standard is applicable to situations in which such data is recorded on or transported by patient healthcards compliant with the physical dimensions of ID-1 cards defined by ISO 7810. This draft International standard specifies the basic structure of the data contained within the medication data object , but does not specify or mandate particular data-sets for storage on devices. The porpuse of this standard is for cards to provide information to other health professionals and to the patient or ist non-professional care giver. It may also be used to carry a new prescription from the prescriber to the dispenser/pharmacy in the design of ist sets. Medication data includes the following four components:-Medication notes, the list of all medication for a patient;-Medication prescriptions, to carry a new prescription from the prescriber to the dispenser/pharmacy;-Medication dispensed, the records of medications bought by the patient;-Medication references, pointers to other systems that contain information that makes up an medication prescription and the authority to dispense. In order to facilitate interoperability, whenever an application is built for use in the healthcare domain in compliance with this Draft International Standard, data items required for that application shall be drawn from the list of objects (some of which are extensible) as provided in clauses 6 to 8. These shall then be used in conjunction with other data defined in other parts of this Draft International Standard.The detailed functions and mechanisms of the following services are not within the scope of this Draft International standard, (although its structures can accommodate suitable data objects elsewhere specified):-the encoding of free text data;security functions and related services which are likely to be specified by users for data cards depending on their specific application, for example:-confidentiality protection, data integrity protection, and authentication of persons and devices related to these functions;-access control services which may depend on active use of some data card classes such as microprocessor cards;-the initialisation and issuing process (which begins the operating lifetime of an individual data card, and by which the data card is prepared for the data to be subsequently communicated to it according to this Draft international standard). The following topics are therefore beyond the scope of this Draft international standard:-physical or logical solutions for the practical functioning of particular types of data cards;-how the message is processed further .downstream. of the interface between two systems;-the form which data takes for use outside the data card, or the way in which such data is visibly represented on the data card or elsewhere. It should be noted that not only the definition of .medicinal products. differs from country to country, but also even the same name of the product does not indicate same product in some countries. Therefore special attention should be made when the card is used across the border for the safety of patient. As a matter of course, exchange of prescription across the boarder should follow all instructions, rules, terms and treaties between the said two countries.


ICS-code 35.240.80
Nederlandse titel Medische informatica - Patiëntgezondheidskaart gegevens - Deel 7: Elektrionisch voorschrijven (medicatie data)
Engelse titel Health informatics - Patient healthcard data - Part 7: Electronic prescription (medication data)
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