Standard Svensk standard · SS-EN ISO 13408-1:2011/A1:2013

Aseptisk behandling av medicintekniska produkter - Del 1: Allmänna krav (ISO 13408-1:2008/Amd 1:2013)

Status: Upphävd

· Ersätts av: SS-EN ISO 13408-1:2015
Omfattning
1.1 This part of ISO 13408 specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing process for aseptically-processed health care products. 1.2 This part of ISO 13408 includes requirements and guidance relative to the overall topic of aseptic processing. Specific requirements and guidance on various specialized processes and methods related to filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in other parts of ISO 13408. NOTE This part of ISO 13408 does not supersede or replace national regulatory requirements, such as Good Manufacturing Practices (GMPs) and/or pharmacopoeial requirements that pertain in particular national or regional jurisdictions.

Ämnesområden

Sterilisering och desinficering allmänt (11.080.01) Desinficeringsmedel och antiseptika (11.080.20) Farmakopéprodukter allmänt (11.120.01)


Produktinformation

Språk: Engelska

Framtagen av: Rengöring, desinfektion och sterilisering, SIS/TK 349

Internationell titel: Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)

Artikelnummer: STD-90062

Utgåva: 1

Fastställd: 2013-05-13

Antal sidor: 20

Tillägg till: SS-EN ISO 13408-1:2011

Ersätts av: SS-EN ISO 13408-1:2015