Valsts valodas centra izstrādātie medicīnas zinātņu, farmācijas un veterinārmedicīnas termini

Konteksts: [..] For blood screening devices (with the exception of HBsAg tests), all true positive samples shall be identified as positive by the device to be CE marked (Table 1). [..]
Avots: Commission Decision of 7 May 2002 on common technical specifications for in vitro-diagnostic medical devices (notified under document number C(2002) 1344) (Text with EEA relevance) (2002/364/EC)