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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

Bovine Spongioform Encephalopathy (BSE) - Use Reagent Grade Materials of Bovine Origin Med Practice

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