DIN EN ISO 13408-1
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008 + Amd 1:2013); German version EN ISO 13408-1:2011 + A1:2013
Aseptische Herstellung von Produkten für die Gesundheitsfürsorge - Teil 1: Allgemeine Anforderungen (ISO 13408-1:2008 + Amd 1:2013); Deutsche Fassung EN ISO 13408-1:2011 + A1:2013
Overview
This amendment (EN ISO 13408-1:2011 + A1:2013) has been prepared by Technical Committee ISO/TC 198 "Sterilization of health care products" in collaboration with Technical Committee CEN/TC 204 "Sterilization of medical devices". The responsible German committee is Working Committee NA 063-01-12 AA "Aseptische Herstellung" ("Aseptic processing") of the Medical Standards Committee, NAMed. The amendment primarily concerns a revision of Figure A.1 in Annex A relating to requirements for cleanroom conditions for fitting caps as well as an update of the normative references.
Document: references other documents
Document: referenced in other documents
Responsible national committee
NA 176-03-10 AA - Aseptic processing
Responsible european committee
CEN/TC 204 - Sterilization of medical devices
