Designed around the way
your specialty works.
Linked participants and consent roles → treatment cycle → individual gametes/embryos → transfer and outcome.
Register partners/donors/gestational carrier as distinct people with permissioned relationships; capture fertility history, investigations and cycle plan.
Coordinate stimulation calendar, prescriptions, serial follicles/hormones, trigger and retrieval timestamps, semen collection and preparation.
Embryology workspace tracks oocyte maturity, insemination/ICSI, fertilization, individual embryo observations, biopsy shipment and genetic reports.
Record transfer, luteal support plan, cryostorage movements and outcome follow-up; maintain consumable lots and witness events at critical transitions.
Diagnosis coverage and clinical records
Male-factor infertility; ovulatory dysfunction; tubal disease; endometriosis-associated infertility; diminished ovarian reserve; unexplained infertility; fertility preservation indication. Record indication independently of cycle outcome and avoid inferring diagnosis from a single reserve test.
Measurements that give the record meaning
| Measurement | Units / representation | Clinical context |
|---|---|---|
| Follicles by ovary | count; mm | Individual measurements, scan date and cycle day |
| Endometrial thickness | mm | Pattern and scan method |
| Estradiol, LH and progesterone | assay-specific units | Collection relative to medication/trigger |
| AMH and antral follicle count | ng/mL or pmol/L; count | Assay and age context |
| Semen analysis | mL; million/mL; % | Collection, abstinence interval, method and reference edition |
| Oocytes/embryos | counts and categorical grades | Individual IDs, maturity, pronuclei, day/hour and grading system |
| Embryo development timings | hours | Reference event, incubator clock and observation source |
Equipment and integration plans
- Time-lapse incubator/EmbryoViewer → authorized embryo-linked exports; EmbryoScope 8 is a candidate, not a verified FertPro connector.
- Electronic witnessing → patient/cycle/sample identifiers and event acknowledgements; Vitrolife describes an EMR API, requiring contract and validation.
- Ultrasound, hormone analysers, CASA and laser/biopsy workstations → images/results/procedure records via appropriate vendor interface.
Connections require an approved interface and testing against the installed manufacturer, model and software. Listed equipment is a candidate integration target.
Explore equipment & roboticsReporting and meaningful outcomes
Fertilization rate with mature/inseminated denominator explicitly chosen; blastocyst formation by cohort; live birth per initiated cycle and per transfer reported separately with follow-up completeness.
Development scope and clinical validation
Initial scope
Cycle scheduling, monitoring, embryology lineage, witnessing records, transfer and outcome register.
Advanced scope
Time-lapse data, e-witness API, biopsy/genetics and validated multi-clinic reporting.
Example acceptance scenarios
- A mismatched person, dish or embryo must block the affected electronic transition and create an exception record.
- A failed interface cannot be marked witnessed; manual witnessing requires the approved fallback process and later reconciliation.
Research foundations
Research snapshot: 23 September 2026. References inform the proposed design; they do not certify FertPro or establish device compatibility. Diagnosis lists and measurement groups are not treatment protocols.