We help healthcare providers, laboratories, and diagnostic organisations deliver accurate, high-quality genetic services — from lab setup to clinical strategy.
We are specialists in clinical genetics and genomic medicine, working with healthcare organisations, diagnostic labs, and life science companies across the UK and Europe.
Our team combines deep clinical knowledge with hands-on operational experience — so our advice doesn't just make scientific sense, it actually works in practice.
Whether you need to build a lab from scratch, interpret complex genomic data, or develop a sustainable business model for diagnostics, we've done it before.
Expert-level knowledge across genetics, molecular diagnostics, oncology, reproductive health, and pharmacogenomics.
Deep familiarity with ISO 15189, UKAS, CQC, and international accreditation standards. We guide you through compliance — without the guesswork.
We don't just advise. We help you build, scale, and sustain services that are commercially viable and clinically excellent.
From strategic consulting to hands-on lab development, we cover every stage of the genomic services lifecycle.
Expert consulting across modern genomic technologies — from NGS and SNP arrays to NIPT, PGD, and oncology screening. We support accurate interpretation and clinical decision-making.
End-to-end support for building or optimising clinical labs — facility design, equipment selection, workflow, staffing, and full ISO 15189 quality management implementation.
Specialist advisory services across clinical genetics, molecular diagnostics, and reproductive medicine. Includes independent expert reviews and second opinions on complex cases.
Strategic support for launching, scaling, and optimising diagnostic services. From market entry to commercial positioning, pricing strategy, and leadership advisory.
Design and implementation of pharmacogenomics testing programmes — integrating genetic insights into clinical workflows to enable truly personalised medicine.
High-level programmes for clinicians, scientists, and lab personnel. Includes workshops, MSc and PhD-level academic teaching, and postgraduate research mentorship.
Support for achieving and maintaining accreditation — audit preparation, QA system development, risk management, and continuous improvement aligned with international standards.
We work exclusively in genetics and genomics. No generalists. No off-the-shelf frameworks. Every engagement draws on real, domain-specific expertise.
We know what auditors look for. From ISO 15189 to UKAS and CQC, we guide you through compliance with clarity and precision.
From concept to operation, we stay involved. You get consistent support — not a report dropped in your inbox and no follow-through.
Scientific excellence has to be sustainable. We help you build services that are clinically sound and financially viable.
We start with a focused conversation to understand your goals, challenges, and current situation — no assumptions, no jargon.
You receive a clear, tailored proposal — outlining scope, timeline, and deliverables. No hidden fees or ambiguity.
We work with your team directly — whether in-person, remote, or hybrid — adapting to your environment and pace.
Deliverables are built to be used — not archived. We ensure knowledge transfer and continued support where needed.
Our clients include NHS and private healthcare providers, diagnostic laboratories, biotech companies, insurers, academic institutions, and healthcare startups. If you work in or around genomics, we can likely help.
Yes. We work with organisations across the UK, Europe, and beyond. Our regulatory knowledge covers UK and international frameworks, and we're experienced in cross-border service development.
Absolutely. We work with organisations just starting out as well as established services looking to optimise. We tailor our involvement to where you actually are, not where you should be.
Every project is different, but most begin with a scoping phase, move into active consulting or implementation, and end with a clear set of deliverables and a handover plan. Duration ranges from a few weeks to several months.
Yes. Many clients retain us on an advisory basis after the initial engagement. We're happy to discuss flexible ongoing arrangements that suit your needs and budget.
Yes. We regularly provide independent second opinions and expert case reviews for complex genetic diagnoses — useful for clinical teams, legal contexts, or quality assurance purposes.
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