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Glavni meni

ISO 11616:2012

Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information
26. 10. 2012.
95.99   Povučen   19. 10. 2017.

Опште информације

95.99     19. 10. 2017.

ISO

ISO/TC 215

Međunarodni standard

35.240.80  

engleski   francuski  

Kupovina

Povučen

Jezik na kome želite da primite dokument.

Apstrakt

ISO 11616:2012 is intended to provide specific levels of information relevant to the identification of a medicinal product or group of medicinal products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, ISO 11616:2012 is essential to ensuring that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders. This ensures interoperability and compatibility for both the sender and the recipient.

Životni ciklus

TRENUTNO

POVUČEN
ISO 11616:2012
95.99 Povučen
19. 10. 2017.

REVIDIRAN OD

OBJAVLJEN
ISO 11616:2017

Nacionalna preuzimanja

Informatika u zdravstvu — Identifikacija medicinskih proizvoda — Elementi i strukture podataka za jedinstvenu identifikaciju i razmenu regulisanih informacija o farmaceutskim proizvodima

95.99   Povučen