Female Hormone Checkup Profile at ₹1,999 | Test List and Details

• 1) Chat on WhatsApp: Share name and age, area PIN code, complete address, and preferred date and time for home sample collection appointment.
• 2) Sample collection: Certified phlebotomist will visit your address with sterile kits as per your convenience.
• 3) Processing: Samples will transported to Thyrocare’s NABL-accredited lab with automated cold-chain logistic.
• 4) Reports: Digital reports delivered securely; consult your doctor for clinical decisions.

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End-to-end cold-chain handling, standardized analyzers, multi-level internal QC, and periodic external quality assurance. Reports include reference ranges and flags where applicable.

NABL accreditation • Barcode traceability • Tamper-evident vacutainers

• Basic hormone panels: Same-day reporting (12-24 hours).
• Advanced & Comprehensive panels: 48–60 hours from the time of sample collection.
• PCOD/PCOS integrated panel: 72–84 hours from the time of sample collection.

You can download partial report before the full processing get completed.

• Clear identifiers: barcode and labcode for specimen traceability.
• Sample handling timestamps: SCT (collection time), SRT (lab receiving time), RRT (report release time).
• Per-test details: value, units, method/technology (e.g., HPLC/CLIA/ELISA/LC-MS/MS), and reference ranges.
• Derived markers: indices calculated from primary values (example: ABG from HbA1c; insulin resistance indices from fasting glucose + fasting insulin).
• Interpretation guardrails: reference ranges are method-specific; results are for clinician interpretation; re-check is advised if an unexpected abnormality appears.

• Barcode: specimen identity number tied to your sample.
• Labcode: lab accession number used for archiving and retrieval.
• SCT: specimen collection time (when blood was collected).
• SRT: specimen receiving time at the laboratory.
• RRT: report releasing time (when values are released for reporting).

These fields help validate chain-of-custody and turnaround context for time-sensitive analytes.

The report prints the technology used for each analyte (example: HbA1c by HPLC, several hormones by CLIA/ELISA, and selected steroid/vitamin markers by LC-MS/MS depending on the panel). Reference ranges are interpreted in the context of the stated method.

If you repeat monitoring, using the same lab/method improves comparability across visits.

Each test line shows value + unit, plus a reference interval. Reference ranges can be age-specific, sex-specific, phase-specific (follicular/luteal), or pregnancy-trimester-specific for selected markers.

• AMH: reference intervals are shown across female age bands (ovarian reserve context).
• TSH (Ultrasensitive): pregnancy trimester ranges are displayed for clinical correlation.
• Lipid parameters: fasting requirement is explicitly flagged where applicable.

Any out-of-range value must be interpreted with symptoms, cycle day/pregnancy status, medications, and clinician judgment.

• ABG (Average Blood Glucose): calculated from HbA1c for glucose control context.
• FAI (Free Androgen Index): derived from Total Testosterone and SHBG.
• HOMA-IR: insulin resistance index derived from fasting insulin and fasting glucose (with a normal cut-off printed on report).
• Quantitative Insulin Sensitivity Index: a derived index with interpretive thresholds printed on report.

These indices are supportive markers; they do not replace clinical diagnosis.

The report prints the specimen type for each group of tests, such as SERUM for many hormone assays, EDTA for hematology, and FLUORIDE for glucose stabilization in fasting glucose testing. This improves transparency on pre-analytical handling.