NEN ISO 13022 : 2012
Current
Current
The latest, up-to-date edition.
MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES
Published date
12-01-2013
Publisher
Sorry this product is not available in your region.
Defines requirements and guidance for processing practices and managing risk associated with viable cellular components of products regulated as medicinal products, biologics, medical devices and active implantable medical devices, or combinations thereof.
| DocumentType |
Standard
|
| PublisherName |
Netherlands Standards
|
| Status |
Current
|
| Standards | Relationship |
| ISO 13022:2012 | Identical |
Summarise
Sorry this product is not available in your region.