Early detection for effective disease management.
Your baby’s first step to a healthy life.
Did You Know?
Early screening empowers timely detection and informed care decisions -helping you better prepare for and manage potential health conditions that may impact your baby’s long-term well-being.
Early Detection for Effective Disease Management.
You and Your Family’s First Step to a Healthy Life.
CORDLIFE NIPT: SUITABLE AS EARLY AS 10TH WEEK OF PREGNANCY
From a simple blood draw as early as 10 weeks into your pregnancy, NIPT services screens for the most common chromosomal abnormalities that can affect your developing baby’s future.
CORDLIFE CMA: A FIRST-TIER DIAGNOSTIC TOOL THAT COMPLEMENTS NIPT
A confirmatory test that can detect chromosomal abnormalities using amniotic fluid, buccal swab, or whole blood.
CORDLIFE BABY GENETIC SCREENING: SUITABLE FOR NEWBORNS AND KIDS UP TO 6 YEARS OF AGE
Using SNP chromosomal microarray technology, Cordlife Baby Genetic Screening can identify more than 241 conditions caused by chromosomal abnormalities and disease-causing gene variants, providing you an expanded insights of your baby’s health condition.
CORDLIFE CLINICAL LABORATORY SERVICES: HOME SERVICE TESTS
Committed to supporting the holistic journey of pregnant women and families, Cordlife Philippines offers premium go-to home service clinical laboratory services.
About Cordlife Philippines
Beyond cord blood, cord lining and cord tissue banking, Cordlife is committed to offer a comprehensive suite of diagnostics services for the customer and their family including Non-invasive Prenatal Testing, Chromosomal Microarray Analysis Test, and Baby Genetic Screening.
