AAMI TIR50:2014(R2017)
Current
The latest, up-to-date edition.
Post-market surveillance of use error management
Hardcopy , PDF
English
06-12-2017
Important note : Users cannot be edited or removed once added to your Multi user PDF.
The guidelines described in this technical information report (TIR) are not separate from or in opposition to the existing U.S. Food and Drug Administration’s (FDA’s) and other regulatory bodies' reporting protocols for product failure or adverse events (concerning morbidities or mortalities), which already have standardized protocols.
| DocumentType |
Standard
|
| ISBN |
978-1-57020-514-9
|
| Pages |
46
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Current
|
| Supersedes |
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