Our Preimplantation Genetic Testing (PGT ) service tests for genetic abnormalities in embryos before implantation. By analysing the genetic makeup of embryos, your clinic can preferentially select healthy embryos for transfer. We offer PGT for the detection of embryos with an abnormal number of chromosomes (PGT-A), as well as testing embryos for a known familial genetic condition (PGT-M), or structural rearrangement (PGT-SR).

Discover the safety and efficacy of our NIPT in evaluating the likelihood of chromosomal abnormalities like Down syndrome, Edwards syndrome, and Patau syndrome in your baby. Our non-invasive screening method ensures no risk to you or your baby, employing cutting-edge technology to analyse DNA extracted from a simple blood sample taken from your arm. Gain valuable insights into the chromosomal health of your unborn baby through our advanced and risk-free screening process.

POCScreen is a comprehensive test tht analyses the tissue from a pregnancy loss to determine if the loss is due to a chromosomal abnormality. The purpose of the POCScreen test is to give you information about the possible cause of the pregnancy loss. The screening also provides you with the insights your healthcare provider needs for reproductive planning.

Our fertility services are designed to help you take the first steps towards your family's future.

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