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Bovine Spongioform Encephalopathy (BSE) - Use Reagent Grade Materials of Bovine Origin Med Practice
Doc type: Policy Directive Compliance with this policy directive is mandatory.
Doc No.: PD2005_200
Functional Group - Sub Group: Clinical/ Patient Services - Pharmaceutical
Summary
Directs hospitals to not use bovine derived materials in areas of medical practice unless the material has been evaluated by the TFA and has been included on the ARTG.
Date of Publication: 27 January 2005
Replaces: N/A
Author Branch: Pharmaceutical Services
This document applies to: Area Health Services/Chief Executive Governed Statutory Health Corporation, Board Governed Statutory Health Corporations, Affiliated Health Organisations - Non Declared, NSW Ambulance Service, NSW Dept of Health, Public Hospitals
Distributed to: Public Health System, NSW Ambulance Service , NSW Department of Health, Public Hospitals
Review Date: 27 January 2010
File No: 01/3892
Previous reference: 2001/48
Issue Date: 15 June 2001
Status: Active
File link: Bovine Spongioform Encephalopathy (BSE) - Use Reagent Grade Materials of Bovine Origin Med Practice
File size: 27Kb
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