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General requirements for in vitro diagnostic medical devices for self-testing
60.60 Standard published
Performance evaluation of in vitro diagnostic medical devices
60.60 Standard published
Performance evaluation of in vitro diagnostic medical devices
60.60 Standard published
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
60.60 Standard published
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
60.60 Standard published
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
60.60 Standard published
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
60.60 Standard published
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003)
60.60 Standard published
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing
60.60 Standard published
In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, tests
60.60 Standard published
Biological evaluation of medical devices — Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process
40.60 Close of voting
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