Nota: Devi essere registrato per rispondere al messaggio. Per registrarti, clicca qui. La registrazione è GRATUITA!
R E V I S I O N E D E L L A D I S C U S S I O N E
swpt_EtTLIZ1D
Inviata - 01/08/2020 : 22:33:45 1. Purpose The purpose of this proposal is to provide an validation of the analytical sensitivity. The production of at least three consecutive 2019-nCOV IgG/IgM Rapid Test Device products shall be controlled.
3. Material Positive Control:2019-nCOV-IgM; Positive Control:2019-nCOV-IgG; Validation lot 1:NO1G01T; Validation lot 2:NO1G02T; Validation lot 3:NO1G03T.
4. Method Tests the low positive control of 2019-nCOV-IgM,2019-nCOV-IgG and negative sample.Each specimen tests in 11 tests.Read the positive result at 10 min.Do not interpret the result after 15 minutes.
5. Interpretation of results Positive result:≥G3 Negative result:<G3