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BSI - BS PAS 84

Regenerative medicine - Glossary

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Organization: BSI
Publication Date: 30 April 2008
Status: inactive
Page Count: 38
ICS Code (Medical sciences and health care facilities in general): 11.020
ICS Code (Health care technology (Vocabularies)): 01.040.11

Document History

BS PAS 84
March 30, 2012
Cell therapy and regenerative medicine – Glossary
A description is not available for this item.
BS PAS 84
April 30, 2008
Regenerative medicine - Glossary
A description is not available for this item.
PAS 84
April 30, 2008
Regenerative medicine - Glossary
A description is not available for this item.

References

This document references:
ASTM F2312 - Standard Terminology Relating to Tissue Engineered Medical Products
Published by ASTM on April 1, 2011
This terminology defines basic terms and presents the relationships of the scientific fields related to Tissue Engineered Medical Products (TEMPs). Committee F04 has defined these terms for the...
This document references:
BS EN ISO 14644-1 - Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration
Published by BSI on January 31, 2016
A description is not available for this item.
This document references:
BS EN ISO 10993-6 - Biological evaluation of medical devices Part 6: Tests for local effects after implantation
Published by BSI on December 31, 2016
A description is not available for this item.
This document references:
BS PAS 83 - Developing human cells for clinical applications in the European Union and the United States of America – Guide
Published by BSI on June 30, 2012
A description is not available for this item.
This document references:
2001/20/EC - Directive of the European Parlament and of the Council on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use
Published by EU on April 4, 2001
A description is not available for this item.
This document is referenced by:
ISO 13022 - Medical products containing viable human cells - Application of risk management and requirements for processing practices
Published by ISO on April 1, 2012
This International Standard specifies requirements and guidance for processing practices and managing risk associated with viable cellular components of products regulated as medicinal products,...
This document is referenced by:
BS PAS 93 - Characterization of human cells for clinical applications. Guide
Published by BSI on August 31, 2011
A description is not available for this item.
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