Council Directive of 22 December 1986 Amending Directive 75/318/EEC on the Approximation of the Laws of the Member States Relating to Analytical, Pharmaco-Toxicological and Clinical Standards and Protocols in Respect of the Testing of Proprietary Medicinal Products
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices (Consolidated 2020), amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
Information technology - Data interchange on 90 mm flexible disk cartridges using modified frequency modulation recording at 31 831 ftprad on 80 tracks on each side - ISO Type 303
Information technology - 3,81 mm wide magnetic tape cartridge for information interchange - Helical scan recording - DDS-DC format using 60 m and 90 m length tapes