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Description of BS EN ISO 22442-3:2007 2008This part of ISOÂ 22442 specifies requirements for the validation of the elimination and/or inactivation of viruses and TSE agents during the manufacture of medical devices (excluding in vitro diagnostic medical devices) utilizing animal tissue or products derived from animal tissue, which are non-viable or have been rendered non-viable. It applies where required by the risk management process as described in ISOÂ 22442-1. It does not cover other transmissible and non-transmissible agents.
This part of ISOÂ 22442 does not cover the utilization of human tissues in medical devices. This part of ISOÂ 22442 does not specify a quality management system for the control of all stages of production of medical devices.
This part of ISOÂ 22442 does not consider the effect of any method of elimination and/or inactivation on the suitability of the medical device for its intended use.
About BSIBSI Group, also known as the British Standards Institution is the national standards body of the United Kingdom. BSI produces technical standards on a wide range of products and services and also supplies certification and standards-related services to businesses. |
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