Patient identity
Name, primary file number, full date or year of birth, nationality, identity and contact information.
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Name, primary file number, full date or year of birth, nationality, identity and contact information.
Link husband and wife records and recall their details in couple-based procedures, without a separate patient file number for every test.
Case register, new entry and active cases; reopen saved work to continue.
Save and resume later, or close completed cases after checks in supported workflows.
Open or delete active cases according to permissions, with in-app confirmation and no deletion of the master patient record.
Collection location, abstinence, a shared date, collection time and examination time.
Volume, colour, viscosity, liquefaction and gelatinous material, with notes.
Manually entered numeric value, or less than 100,000/mL with a written description.
Numeric or less-than-1% modes with descriptive text; progressive and non-progressive motility and morphology.
Total count from volume and concentration, and total motility from motility inputs when calculable. Record agglutination, aggregation, round and epithelial cells and debris.
Enter assessed and fragmented sperm counts to calculate the percentage, with sample details, team and notes.
Add sample-linked cryopreservation with date, vial count, location and team. This option is not part of DFI.
Procedure, biopsy and side-specific details, descriptive findings, final results and report notes, with doctor, laboratory staff and witness selected from lists.
Select the couple, procedure date and collection and preparation times. First and optional second samples, pre- and post-preparation findings, preparation methods, team and notes.
Case date, trigger date and time, doctor, marriage duration, children and previous attempts with details and notes.
Record media and batch numbers, adding further media entries with their corresponding batches when needed.
Fresh or frozen; ejaculate, FNA or TESE, with an optional second sample and descriptive assessment where appropriate.
Direct Swim up, Wash, Swim up+Wash, Density Gradient, Sperm Ship and Others with optional text, plus post-preparation findings.
Oocyte count, retrieval time, doctor, embryologist, witness and notes, with procedures anchored to the case date.
Choose IVF, ICSI or both; separate counts and times, recording denudation, injection and remaining or unallocated oocytes.
Classify GV, MI, degenerated, atretic and other oocytes. Record 0PN, 1PN, 2PN, 3PN and Multi PN with count-consistency checks.
Individual or grouped assessment: embryo count, cell count and grades 1–4, with additional groups. Day-4 assessment is optional.
Individual or grouped day-5 assessment: expansion 1–6, ICM and TE grades A, B and C, with stage and embryo notes.
Add one or more biopsy events with day, retrieval-based date, time, embryos, requested test, team and genetics laboratory.
Document rebiopsy, the relevant embryo and reason where supported, and link diagnosis results to the register.
Embryo day, transfer date and time, selected embryos, doctor, embryologist, witness, catheter, media and notes.
Record no transfer, cryopreservation or diagnosis before transfer, and add case-linked cryopreservation events.
Documentation options for Embryo Glue, LAH, IMSI, PICSI, Time-lapse and Others. These record techniques; they do not perform them automatically.
Standalone or case/biopsy-linked diagnosis, with couple, diagnosis date and embryo count.
PGT-A, PGT-M, PGT-SR, FISH or Other, with an optional laboratory report number.
Euploid, aneuploid, mosaic, no result, inconclusive or other findings, with detail, disposition and reason. Results are entered from the report, not generated as an automated diagnosis.
Sperm, oocytes, embryos and ovarian tissue, each with a relevant register and fields.
Patient, sample, date and internal or external source according to form; vials or straws, Tank / Can / Sleeve location, team, notes and attachments.
Embryo count per straw, cryopreservation day and grades, with linked embryo detail where supported.
Use, transfer or disposal with date, quantities and notes, updating remaining stock.
Reverse an action in permitted workflows with a reason, retaining the previous action in the record.
Track storage renewal and automatically record outstanding storage years, alongside renewal status, follow-up, authorisations and attachments.
View the patient’s inventory and select samples or straws. Recording thawing updates stock and adds a sample action; saving draft selections alone does not complete thawing.
Fully Survived, Partially Survived or Not Survived for each thawed embryo.
Allocate transfer, re-cryopreservation and disposal; non-survivors count as discarded, not surviving remainder. Re-cryopreserved embryos are added to the register with location details.
Manually enter survived and non-survived counts that reconcile with the thawed oocyte total.
Link the couple before ICSI, then preparation, fertilisation, embryo follow-up, diagnosis, transfer or freeze-all as applicable, including a no-transfer outcome.
Draft, submit for review, confirm review, approve and reopen with a reason in supported workflows and according to permissions.
Print, save PDF and export Excel tables according to record type and permissions, and compare previous semen analyses in the dedicated section.
Identity documents, consents, reports and images in PDF, JPG/JPEG, PNG and WebP, up to 25 MB per file, linked to the patient record or case.
An individual patient or couple, date and time, doctors and staff, manual procedure descriptions and notes, with optional attachments.
Procedure counts, active and completed cases, date-range and procedure filters, search and monthly activity.
Show remaining embryos, oocytes and vials in their own units. These are operational indicators, not clinical success rates; current stock is not a historical period-end balance.
Manage doctors, staff and users, select them from registered lists, and control viewing, entry, editing, approval and export permissions.
Centre name and logo, Arabic and English interfaces, and custom quick-access visibility, order and icons.
Audit history, institution settings, backup and restore tools, and centre-network settings according to edition.
Details are based on the product catalogue and documented workflows. Fields depend on procedure, release, settings and permissions; request a demonstration to confirm your centre’s workflow.
Tell us how your laboratory works, and we can walk through the details in the application.
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