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Farrukh Jamil GRW-10: Rahwali Cantt Blue Card Out of station 20%
68601-19-104499166
Age/Sex : Registration Date: Consultant: Case Number:
30 (Y) / M 28-Jun-2022 21:00 DR SUJERA YASMEEN 35321-28-06
Note : ,,,,
Specimen Plasma
Electronically verified report. No signature required. Lab reports should be interpreted by a physician in correlation with clinical and radiologic findings.
Result Not Detected
Comments :
This test performed on the cobas® 6800 System.
This test is based on fully automated sample preparation (nucleic acid extraction and purification) followed by
PCR amplification and detection.
This test is an in vitro reverse transcription polymerase chain reaction (RT-PCR) assay for the quantitation of
hepatitis C viral ribonucleic acid (HCV RNA) in human plasma from HCV-infected individuals.
This test is intended for use as an aid in the diagnosis of active viral infection.
Note: Two lab intercomparison cannot be done due to difference in sample collection, transportation,
storage, sensitivity and specificity of assay.
Dr. N. A. Malik Dr. Ayisha Imran Prof Waheed UZ Tariq Dr. Omar Chughtai Dr. A . S. Chughtai
M.B.B.S. (Pb) , M. Phil. M.B.B.S., F.C.P.S. M.B.B.S., PhD. DpBact M.B.B.S., M.D., F.C.A.P. M.B.B.S., M.I.A.C., M.Phil.
Consultant Haematologist Consultant Haematologist F.C.P.S, F.R.C.Path, F.R.C.P.EConsultant Diplomate American Board of Anatomic F.C.P.S., F.C.P.P.Consultant Pathologist
Virologist and Clinical Pathology
Specimen Plasma
Electronically verified report. No signature required. Lab reports should be interpreted by a physician in correlation with clinical and radiologic findings.
Result Not Detected
Comments :
This test performed on the cobas® 6800 System.
This test is based on fully automated sample preparation (nucleic acid extraction and purification) followed by
PCR amplification and detection.
This test is an in vitro reverse transcription polymerase chain reaction (RT-PCR) assay for the quantitation of
hepatitis C viral ribonucleic acid (HCV RNA) in human plasma from HCV-infected individuals.
This test is intended for use as an aid in the diagnosis of active viral infection.
Note: Two lab intercomparison cannot be done due to difference in sample collection, transportation,
storage, sensitivity and specificity of assay.
Dr. N. A. Malik Dr. Ayisha Imran Prof Waheed UZ Tariq Dr. Omar Chughtai Dr. A . S. Chughtai
M.B.B.S. (Pb) , M. Phil. M.B.B.S., F.C.P.S. M.B.B.S., PhD. DpBact M.B.B.S., M.D., F.C.A.P. M.B.B.S., M.I.A.C., M.Phil.
Consultant Haematologist Consultant Haematologist F.C.P.S, F.R.C.Path, F.R.C.P.EConsultant Diplomate American Board of Anatomic F.C.P.S., F.C.P.P.Consultant Pathologist
Virologist and Clinical Pathology