Laboratory Infrastructure

Congenital Adrenal Hyperplasia (CAH) includes a group of disorders in which the cortisol production by adrenals is lowered. Cortisol is a steroid hormone necessary to maintenance of blood sugar level, partial maintenance of body fluids and electrolytes and protection of the body against stress. CAH cannot be cured, but it can be effectively treated by steroid substitution therapy if detected in early stage of life and disease course.

• Training Mechanical Trimming Function (10 & 50 μm)
• Specimen Retraction
• Service-friendly
• Low maintenance design
• Quick release specimen clamping
• Quick locking lever

Biocard Troponin I is a qualitative rapid immuno chromatographic test for the detection of cardiac Troponin I from intravenous blood or serum samples

Fully Automated Microbial Culture System

Biocard Parvo B 19 is a onestep immuno chromatographic test for the rapid and convenient screening of Parvovirus B 19 antibodies specific for acute phase of disease in serum plasma or whole blood sample swab sample.

1.Compact Design

2. Quantitative UPLC – MS/MS applications

3. Rapid, reliable and reproducible quantitative data for the clinical laboratory

4. Clinical laborataries have access to the selectively, sensitivity and versatility of LC-MS

5. Reduces complexity and maximizes throughput and uptime

6. The system is controlled by Mass Lynx IVD Software

• The broadest available panel of analytes
• Easy sample preparation without derivatization
• More Analytes with less expenses
• Possibility of Automatic Sample Preparation
• 3 levels of blood spots controls – Low, Mid, High
• Unique endogenous level control

Serum free light chain (sFLC) quantification is an effective tool in both diagnosis and monitoring in conjunction with other laboratory and clinical findings for myeloma and related dyscrasias.

• Comprehensive test menus for enzymes, substrates & specific protein parameters.
• Customized & pre-measured pack size configuration.
• Parameter reagents available in ready-to-use liquid, stable & lyophilised powder format.
• Specially designed mono vial [1 ml] reagent range provides ease of convenience in analysis.
• Parameter available with different selection of methods (IFCC or DGKC).
• Reagent provides precise sensitivity, wide measurement range & long shelf life stability.
• Long working reagent & on board stability for precise automated analysis.

Cystic Fibrosis (CF) is an autosomal recessive disorder affecting the lungs, pancreas, intestine and liver. CF is the most common in Caucasians with an incidence rate 1:2500 newborns. CF is caused by mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CTFR) [1,2]. Large-scale neonatal screening for CF is performed by indentification of increased levels of immunoreactive trypsinogen (IRT) in blood.