Molecular Diagnostics

The Final Shop of Molecular Diagnostics Solution




GCC's in vitro diagnostics team has been engaged in a contest against the constant evolution of bacteria, the development of infectious diseases and pandemics. Strong with our protein division and experience in microbiology and molecular biology, it is our role as a companion of laboratories worldwide to stay a step ahead. We do this by providing the widest range of solutions on the market, tools and services to improve productivity and quality and the many innovations that contribute to optimizing different diagnostic laboratory performance every day.

Prenatal Detection

Prenatal diagnosis of Ataxia
Prenatal diagnosis of Haemophilla A and B
Prenatal diagnosis of Spinal Muscular Atrophy (SMA)
Prenatal diagnosis of  α Thalassemia
Prenatal diagnosis of  β Thalassemia
Prenatal diagnosis of Duchene  Muscular Dystrophy (DMD)
Cystic Fibrosis Detection
Phenylketonuria (Homogentisic acid) detection
HLA B27 detection
Down Syndrome detection
Tay Sachs Disease detection
Sickle cell anemia detection
Fragile X Syndrome detection