Test Price
450 AEDโ Home Collection Available
Female Infertility Screening Panel in UAE | 450 AED | DHA-Approved Hormonal Assessment
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accreditation (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM โ 11 PM) with ISO-certified transport.
Clinical Guidance: Complimentary telephonic post-test result interpretation by our DHA-licensed clinical team.
Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Priced at 450 AED with same-day results reported by 8 PM, this panel evaluates ovarian reserve and endocrine function through ultra-sensitive chemiluminescent immunoassay.
Test Overview & Methodology
The Female Infertility Screening Panel quantifies key reproductive hormones โ FSH, LH, Estradiol, Prolactin, TSH, and Anti-Mรผllerian Hormone โ using ultra-sensitive chemiluminescent immunoassay technology to identify endocrine and ovarian reserve disorders. This DHA-endorsed panel requires overnight fasting and blood collection on Day 2โ3 of the menstrual cycle for maximal diagnostic accuracy.
| Feature | DNA Labs UAE Panel | Standard Panel Alternative |
|---|---|---|
| Methodology | Chemiluminescent Immunoassay (Ultra-Sensitive) | Conventional ELISA / Manual RIA |
| Diagnostic Sensitivity | 99.9% (ISO-validated) | 90โ95% |
| Turnaround Time (TAT) | Same day (reported by 8 PM) | 3โ5 business days |
| Home Collection | Yes โ cold-chain VIP phlebotomy (8 AMโ11 PM) | Often clinic visit only |
| Post-Test Guidance | Free telephonic interpretation by DHA physician | No standardized support |
Physician Insight & Safety Protocols
โAs a DHA-licensed General Practitioner, I understand the emotional weight that infertility evaluation carries. This hormonal panel provides a reliable snapshot of ovarian reserve and pituitary function, yet it must be interpreted alongside your clinical history, imaging, and partner evaluation. I strongly recommend scheduling a follow-up consultation to review these results and build a personalized fertility roadmap.โ
โ Dr. Ajay Singh, DHA License: 36234132
Pre-Test Advisory
Medication & Supplement Guidance
Do not discontinue any prescribed medication without direct consultation with your treating physician. Abrupt cessation can severely impact your health. Inform our phlebotomist about all supplements โ especially biotin exceeding 5 mg/day, which may interfere with chemiluminescent assay results and require a 48-hour washout period before blood draw.
Exclusion Criteria & Emergency Red Flags
Clinical Exclusions & Urgent Signs
- Exclusion: Acute febrile illness, ongoing pregnancy (hCG positive), or recent (<4 weeks) use of oral/injectable hormonal contraception without washout period. Patients on biotin supplements >5 mg/day should stop 48 hours before draw.
- ER Red Flags: Seek immediate medical care if you develop sudden severe pelvic pain, heavy vaginal bleeding, vision changes, or symptoms of anaphylaxis (swelling, difficulty breathing) after the blood collection.
Patient FAQ & Clinical Guidance
1. Why must the blood sample be collected on Day 2 or 3 of the menstrual cycle?
Baseline hormone levels obtained on Day 2โ3 provide an accurate reflection of ovarian reserve and pituitary function, free from mid-cycle surges and luteal phase variability, enabling precise diagnosis of disorders like diminished ovarian reserve or PCOS. This standardized timing is recommended by DHA-endorsed clinical protocols.
2. Is fasting absolutely required, and what happens if I eat?
Overnight fasting (8โ12 hours) is essential because food intake can transiently alter prolactin and insulin levels, potentially masking subtle hormonal imbalances and leading to an inaccurate clinical picture. Non-fasting samples may show falsely elevated prolactin, prompting unnecessary repeat testing or misdiagnosis.
3. Can I take my regular supplements or medications before the test?
Certain supplements (especially biotin >5 mg) and medications can interfere with the chemiluminescent immunoassay, causing falsely high or low hormone readings; always inform your physician and our phlebotomist of all substances you are taking to adjust pre-instructions safely. Never stop prescribed drugs without professional approval.
4. How are the results delivered and interpreted?
Results are reported digitally by 8 PM on the same day of collection, accompanied by reference ranges. Every patient receives a complimentary telephonic consultation with a DHA-licensed clinician who explains the hormonal profile in the context of your personal health history and recommends next steps.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License No. 1143 and strictly complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for all patient data handling, storage, and transmission. All clinical laboratory processes adhere to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, ensuring secure digital health records and encrypted result delivery. Patient safety and informed consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability, guaranteeing transparent clinical communication and the highest standard of diagnostic care.
Clinical & Logistical Metadata
| Test Name | Female Infertility Screening Panel |
| Price (AED) | 450 |
| Turnaround Time | Same Day (reported by 8 PM) |
| Sample Type / Matrix | Blood (Serum/Plasma) โ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Chemiluminescent Immunoassay (Ultra-Sensitive) |
| ICD-10-CM Code | N97.9 |
| LOINC Code | 54089-8 |
| DHA Facility License & Laboratory Address | Facility #1143 โ Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE โ DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians