Absolutely. Fertility CDS is specifically designed to support GPs in conducting structured initial fertility assessments before specialist referral. It guides you through evidence-based investigation pathways aligned with NICE and WHO guidelines, helping you identify when to refer, what investigations to order, and how to counsel patients — all without requiring specialist-level training.

A complete structured intake for a couple typically takes 10–15 minutes. The platform uses smart conditional logic, so only relevant questions are shown based on prior answers. The decision engine then generates recommendations instantly, meaning you can complete a full evidence-based fertility assessment within a standard consultation slot.

The platform is aligned with five major international bodies: WHO (World Health Organization), ASRM (American Society for Reproductive Medicine), ESHRE (European Society of Human Reproduction and Embryology), NICE (National Institute for Health and Care Excellence), and ACOG (American College of Obstetricians and Gynecologists). Each recommendation is tagged with its evidence source and guideline version for full auditability.

The risk stratification engine analyses structured intake data and investigation results to categorise couples into three management tiers: (1) Expectant Management — for couples with good prognosis and short infertility duration; (2) IUI Candidates — for couples with mild male factor, unexplained infertility, or cervical factors; (3) IVF/ICSI Referral — for couples with severe male factor, tubal disease, endometriosis, or failed IUI cycles. Each categorisation is evidence-tagged and auditable.

No. Fertility CDS is a Clinical Decision Support (CDS) tool and is not an FDA 510(k)-cleared, MHRA-registered, or CE-marked medical device. It is classified under FDA 2019 CDS guidance and UK MHRA AI/ML guidance as a non-device CDS tool. The platform provides evidence-based recommendations to support clinical judgment, but all clinical decisions remain the responsibility of the treating healthcare professional. The tool is intended for use by licensed healthcare professionals only and does not replace independent clinical evaluation.

Yes. The Pre-ART Optimisation Module provides structured protocols for both female and male partners, covering lifestyle modifications, micronutrient supplementation, weight management, smoking cessation, and medical optimisation (e.g., thyroid correction, glycaemic control). Protocols are evidence-based and can be customised to your clinic's formulary and patient preferences.

Patient data is encrypted at rest and in transit using AES-256 and TLS 1.3 standards. The platform is built on a HIPAA-compliant architecture and is GDPR/UK GDPR-ready, with full data residency options for EU and UK-based clinics. All access is role-based, and a complete audit log is maintained for every data interaction. We never sell or share patient data with third parties. For US clinics, Business Associate Agreements (BAA) are available upon request.

Yes. The Clinical Report Generator produces branded, downloadable PDF reports with full guideline citations suitable for patient records and referral letters. The Research & Analytics Dashboard allows de-identified population-level data export in CSV and JSON formats, making it ideal for audit, quality improvement, and academic research. Enterprise plans include API access for integration with existing EMR/EHR systems.

Yes. Our Enterprise White-Label plan allows fertility centres and hospital networks to deploy Fertility CDS under their own branding, with custom domain, logo, colour scheme, and report templates. You can also configure custom investigation panels and referral pathways to match your centre's specific protocols. Contact our sales team for a tailored demo and pricing.