ANSI/AAMI/ISO 13408-3:2006(R2015)
Current
The latest, up-to-date edition.
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 3: LYOPHILIZATION
Hardcopy , PDF
English
07-13-2015
Glossary of equivalent standards
Committee representation
Background of ANSI/AAMI adoption of ISO 13408-3:2006
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Quality system elements
5 Product definition
6 Process definitions
7 User requirements
8 Validation
9 Routine monitoring and control
Bibliography
Describes requirements for, and offers guidance on, equipment, processes, programs and procedures for the control and validation of lyophilization as an aseptic process.
Committee |
WG 09
|
DocumentType |
Standard
|
ISBN |
1-57020-328-8
|
Pages |
24
|
ProductNote |
Reconfirmed 2015
|
PublisherName |
Association for the Advancement of Medical Instrumentation
|
Status |
Current
|
Supersedes |
Standards | Relationship |
ISO 13408-3:2006 | Identical |
ISO 13408-4:2005 | Aseptic processing of health care products — Part 4: Clean-in-place technologies |
CFR 21(PTS200-299) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 200-299 |
ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
ISO 13408-1:2008 | Aseptic processing of health care products — Part 1: General requirements |
ISO/TS 11139:2006 | Sterilization of health care products Vocabulary |
CFR 21(PTS1-99) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 1-99 |
ISO 9001:2015 | Quality management systems — Requirements |
ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
ISO 13408-5:2006 | Aseptic processing of health care products Part 5: Sterilization in place |
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