BS PAS 84(2008) : 2008
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
REGENERATIVE MEDICINE - GLOSSARY
Hardcopy , PDF
30-03-2012
English
01-01-2008
Foreword
Introduction
1 Scope
2 General
3 Cell and tissue components
4 Non-cellular components
5 Cell and tissue procurement
6 Measurement and analysis
7 Manufacturing and production
8 Clinical trials
Annexes
Annex A (informative) - Regulatory terms
Bibliography
Describes terms and definitions: a) associated with the naming of types of regenerative medicine products and therapies; b) that describe materials, processes, methodologies and applications within regenerative medicine.
| DocumentType |
Standard
|
| Pages |
38
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| BS PAS 93(2011) : 2011 | CHARACTERIZATION OF HUMAN CELLS FOR CLINICAL APPLICATIONS - GUIDE |
| ISO 13022:2012 | Medical products containing viable human cells — Application of risk management and requirements for processing practices |
| 10/30203224 DC : 0 | BS ISO 13022 - MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES |
| ASTM F 2312 : 2011 : REDLINE | Standard Terminology Relating to Tissue Engineered Medical Products |
| BS EN ISO 14971:2012 | Medical devices. Application of risk management to medical devices |
| 2007/47/EC : 2007 COR 1 2015 | DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 5 SEPTEMBER 2007 AMENDING COUNCIL DIRECTIVE 1990/385/EEC ON THE APPROXIMATION OF THE LAWS OF THE MEMBER STATES RELATING TO ACTIVE IMPLANTABLE MEDICAL DEVICES, COUNCIL DIRECTIVE 1993/42/EEC CONCERNING MEDICAL DEVICES AND DIRECTIVE 1998/8/EC CONCERNING THE PLACING OF BIOCIDAL PRODUCTS ON THE MARKET(TEXT WITH EEA RELEVANCE) |
| CFR 21(PTS800-1299) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 800-1299 |
| BS PAS 83(2006) : 2006 | GUIDANCE ON CODES OF PRACTICE, STANDARDISED METHODS AND REGULATIONS FOR CELL-BASED THERAPEUTICS |
| ISO/IEC Guide 51:2014 | Safety aspects — Guidelines for their inclusion in standards |
| BS EN ISO 10993-6:2016 | Biological evaluation of medical devices Tests for local effects after implantation |
| BS EN ISO 14644-1:2015 | Cleanrooms and associated controlled environments Classification of air cleanliness by particle concentration |
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