Six ways to read a pregnancy.
From first-trimester screening to compassionate post-loss investigation — a complete reproductive genetics pathway built on FMF UK and NHS UK protocols and powered by EVICOScreen™.
01 · Prenatal Screening (PNS)
First-trimester risk assessment for the common trisomies and preeclampsia, powered by EVICOScreen™.
- Trisomy 21, 18 & 13 risk estimation
- Preeclampsia risk profiling
- EVICOScreen™ reporting
- FMF UK Nuchal Translucency audit
02 · NIPS / NIPT
Non-invasive prenatal screening reads cell-free fetal DNA from a single maternal blood draw.
- Cell-free fetal DNA analysis
- Non-invasive aneuploidy detection
- Safe for mother and baby
- High sensitivity & specificity
03 · Blood Karyotyping
A whole-genome portrait of chromosomal structure and number.
- Chromosomal structure & number
- Translocations & large deletions
- Trusted, established methodology
04 · Chromosomal Microarray
High-resolution scanning for sub-microscopic imbalances.
- Microdeletions & microduplications
- Resolution beyond karyotyping
- Whole-genome coverage
05 · Next Generation Sequencing (NGS)
Advanced genomic panels reading millions of fragments in parallel.
- Targeted & broad diagnostic panels
- Single-gene to panel-level analysis
- Massively parallel sequencing
06 · Fetal Autopsy
A compassionate, systematic investigation after pregnancy loss.
- Post-loss diagnostic clarity
- Guidance for future pregnancies
- Handled with dignity and care
Screening, engineered.
EVICOScreen™ is our integrated prenatal screening platform — combining biochemistry, ultrasound markers and FMF UK risk algorithms into a single, clinician-ready report.
Guided by leaders in fetal medicine.
Dr. Anita Kaul
Senior expert, fetal medicine & reproductive genetics
Dr. Prathima Radhakrishnan
Fetal medicine & prenatal diagnosis
Dr. Jayaram Kadandale
Cytogenetics & molecular genetics
Not sure which test fits your case?
Our genetic counsellors will walk you and your clinician through the right pathway.