Advanced embryo genetic testing to improve IVF success and reduce inherited risks.
Pre-implantation Genetic Testing (PGT) is performed on embryos created through IVF to identify genetic or chromosomal abnormalities before implantation. This helps optimise embryo selection and improve clinical outcomes.
Testing for chromosomal aneuploidies to improve implantation and live-birth rates.
Testing embryos for single-gene disorders in families with known genetic diseases.
For parents with chromosomal structural rearrangements (e.g., translocations).
Embryo HLA typing to identify compatible donors for affected siblings.
PGT-A Plus offers advanced embryo screening beyond standard aneuploidy testing.
Molecular PN Check confirms the genetic identity of embryos at the pronuclear stage before biopsy.
Embryo parental check ensures accurate matching of embryos to intended parents before genetic testing.
PGT pre‑clinical workup establishes parental genotypes and validates informative markers for embryo testing.
All PGT types follow a structured workflow supporting both clinicians and patients:
While highly informative, PGT has certain limitations and contextual factors:
Speak with our technical team to determine the most suitable PGT option.
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