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Take the first step toward personalized, non-invasive reproductive health insights.
Discover Treatment Strategies Based on Your Unique Genetic Profile
Personalized Medicine uses genetic insights to optimize how your body responds to medications. By analyzing your DNA, this test helps doctors prescribe the most effective drugs at the right doses—minimizing side effects and improving treatment success.
Conditions Detected by Personalized Medicine
01
Drug Response Variability
02
Cancer Therapy Optimization
03
Mental Health Medications
04
Cardiovascular Drug Response
Your Genes, Your Treatment Advantage
Improved Drug Efficacy
Receive treatments that are more likely to work specifically for you.
Reduced Side Effects
Avoid medications your body may react negatively to.
Faster Recovery Path
Minimize the trial-and-error period of finding the right medication.
Proactive Health Decisions
Use genetic insights for lifelong treatment strategies beyond one condition.
How It Works?
Customizing Treatments with Genetic Precision
Genetic Sample Collection
Simple swab or blood sample, collected in our lab or from home.
Pharmacogenomic Analysis
We analyze genes that influence drug absorption, metabolism, and efficacy.
Physician-Guided Report
Receive a comprehensive report with personalized medication recommendations.
Why Choose FSG for this Test ?
01
Advanced Genomic Tools
Utilizing cutting-edge pharmacogenomics technology for high-accuracy results.
02
Expert Clinical Team
Our specialists interpret results to guide precise treatment planning.
03
Fast, Reliable Delivery
Get your full personalized report within a few business days.
04
Pioneers in Precision Medicine
FSG leads personalized diagnostics in the UAE with certified excellence.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
A personalized medicine test analyzes your genetic profile to help tailor medical treatments and lifestyle recommendations that best suit your individual needs.
By understanding your unique genetic markers, the test can identify how you may respond to certain medications, your risk for specific conditions, and guide more effective treatment plans.
Anyone interested in proactive healthcare, especially those with a family history of genetic conditions or individuals looking to optimize treatment effectiveness and avoid adverse drug reactions.
No. The test typically requires a simple blood sample or cheek swab, making it quick and non-invasive.
Results are usually available within 2–3 weeks, depending on the lab processing time. You’ll receive a detailed report with actionable insights.
Non-Invasive Prenatal Testing/Screening
Pre-Implantation Genetic Testing/Screening (PGT/PGS)
Male/Female Fertility
Rapid Prenatal & Pregnancy Loss
Maternal Cell Contamination (MCC)
Product of Conception (POC)
My HLA (Human Leucocyte Antigen)
Whole Genome Sequencing (WGS)
Whole Exome Sequencing (WES)
Low Pass Sequencing (1-3x Coverage)
Comprehensive Oncology Screening
Breast Cancer Screening (BRCA)
Cervical Cancer Screening
Prostate Cancer Screening
Heredity Cancer Panel
Leukemia Panel
Lymphoma Panel
Carrier Screening
Newborn Screening
Infectious Diseases Screening
Rare Diseases Screening
Consumer Genomics
Gut Metagenomics
Metagenomics
Personalized Medicine