Search results
Search list
Results in:
DIN ISO 13022
Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
Edition
2014-06
DIN EN ISO 22442-3
Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007); German version EN ISO 22442-3:2007
Edition
2008-03
DIN EN ISO/IEC 19788-3
Information technology - Learning, education and training - Metadata for learning resources - Part 3: Basic application profile (ISO/IEC 19788-3:2011); German version EN ISO/IEC 19788-3:2013
Edition
2014-03
DIN EN ISO 22442-1
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020); German version EN ISO 22442-1:2020
Edition
2021-08
DIN EN ISO/IEC 19788-2
Information technology - Learning, education and training - Metadata for learning resources - Part 2: Dublin Core elements (ISO/IEC 19788-2:2011); English version EN ISO/IEC 19788-2:2012
Edition
2013-03
DIN EN 15017
Funeral Services - Requirements; German version EN 15017:2019
Edition
2019-11
DIN EN ISO 13408-5
Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006); German version EN ISO 13408-5:2011
Edition
2011-09
DIN ISO 25552
Ageing societies - Framework for dementia-inclusive communities (ISO 25552:2022)
Edition
2024-01
DIN EN ISO 25424
Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018 + Amd 1:2022); German version EN ISO 25424:2019 + A1:2022
Edition
2022-07
DIN EN ISO 13408-2
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018); German version EN ISO 13408-2:2018
Edition
2018-06