Search results
Search list
Results in:
2004/C24/03
Note for guidance on minimising the risk of transmitting animal spongiform encephalopathy agents via human and veterinary medicinal products (EMEA/410/01 Rev. 2 - October 2003) adopted by the Committee for Proprietary Medicinal Products (CPMP) and by the Committee for Veterinary Medicinal products (CVMP)
Edition
2004-01-28
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 58924
Haemostaseology - Reference method for the determination of the collagen binding acitvity of the VWF; Text in German and English
Edition
2022-05
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 16777
Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2, step 2); German version EN 16777:2018
Edition
2019-03
DIN EN 17122
Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase 2, step 2; German version EN 17122:2019
Edition
2020-02
DIN 58987
Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English
Edition
2024-04
DIN ISO 21882
Sterile packaged ready for filling glass vials (ISO 21882:2019)
Edition
2020-12
DIN ISO 21881
Sterile packaged ready for filling glass cartridges (ISO 21881:2019)
Edition
2020-12
DIN EN ISO 11616
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information (ISO 11616:2017); German version EN ISO 11616:2017
Edition
2018-04
