SN EN ISO 27953-1 : 2012
Current
The latest, up-to-date edition.
HEALTH INFORMATICS - INDIVIDUAL CASE SAFETY REPORTS (ICSRS) IN PHARMACOVIGILANCE - PART 1: FRAMEWORK FOR ADVERSE EVENT REPORTING (ISO/DIS 27953-1:2011)
Hardcopy
English
01-06-2012
Important note : Users cannot be edited or removed once added to your Multi user PDF.ISO 27953-1:2011 seeks to establish an international framework for data exchange and information sharing by providing a common messaging format for transmission of ICSRs for adverse drug reactions (ADR), adverse events (AE), product problems and consumer complaints that can occur upon the administration or use of one or more products.
| Committee |
INB/NK 165
|
| DocumentType |
Standard
|
| Pages |
0
|
| PublisherName |
Swiss Standards
|
| Status |
Current
|
| Standards | Relationship |
| EN ISO 27953-1:2011 | Identical |
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