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SN EN ISO 11608-3
Needle-based injection systems for medical use - Requirements and test methods - Part 3: Containers and integrated fluid paths (ISO 11608-3:2022)
Edition
2022-05
SN EN 17229
Fitness centres - Requirements for centre amenities and operation - Operational and managerial requirements
Edition
2019-10
SN EN ISO 17523
Health informatics - Requirements for electronic prescriptions (ISO 17523:2016)
Edition
2016-09
SN EN ISO 20776-1
Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2019, including Corrected version 2019-12)
Edition
2020-12
OENORM EN 16877
Animal feeding stuffs: Methods of sampling and analysis - Determination of T-2 and HT-2 toxins, Deoxynivalenol and Zearalenone, in feed materials and compound feed by LC-MS
Edition
2017-01-15
SN EN 16877
Animal feeding stuffs: Methods of sampling and analysis - Determination of T-2 and HT-2 toxins, Deoxynivalenol and Zearalenone, in feed materials and compound feed by LC-MS
Edition
2017-01
TierZG
Gesetz zur Neuordnung des Tierzuchtrechts sowie zur Änderung des Tierseuchengesetzes, des Tierschutzgesetzes und des Arzneimittelgesetzes (Artikel 1 Tierzuchtgesetz (TierZG))
Edition
2006-12-21
ElekAMInfoMindAnfVÄndV 1
Erste Verordnung zur Änderung der Elektronische Arzneimittelinformationen-Verordnung
Edition
2023-04-19
ApoGuaZustVÄndV NW
Ordinance for the amendment to the ordinance on the competences according to the Pharmacies Act, the Pharmaceutical Products Act, the Narcotics Act, the Federal Regulations on Pharmacies, the Licensing Regulations for Pharmacies, the Act on the profession of pharmaceutic-technical assistants and the training and examination regulations for pharmaceutic-technical assistants
Edition
1982-09-08
EUV 2024/1381
Commission Implementing Regulation (EU) 2024/1381 of 23 May 2024 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medicinal products for human use at Union level, as well as templates for those joint clinical assessments
Edition
2024-05-23
