Science
Medical-adjacent output demands source grounding, refusal patterns and evaluation harnesses. We build them in, not on top.
Life Sciences AI & Digital Delivery
We help pharma, medtech, hospitals and diagnostics vendors design, validate and ship AI systems and digital platforms, from proof-of-concept to production, with data isolation and regulatory-grade robustness as the default.
Trusted by teams across pharma, medtech and hospitals
Novocure
P95
Why Reymont
Most vendors operate in one of these areas. Our engineers have worked inside all three for years, in Tier-1 pharma, university hospitals and biotech instrumentation.
Medical-adjacent output demands source grounding, refusal patterns and evaluation harnesses. We build them in, not on top.
Single-tenant infrastructure, SOC 2 environments, full audit trail. No prompts, responses or documents ever leave the tenant.
Full-stack coverage: LLM backends, RAG, enterprise commerce, niche CMS estates and modern frontends. No framework-of-the-month bias.
Our approach
We do not start with code. We start with your workflow, your data boundaries and the regulatory constraints your reviewers will actually apply.
Workshops with your medical, regulatory and marketing teams. Data inventory, tenant boundaries, model selection and honest scoping, validated before the first line of code.
Isolated cloud (AWS Bedrock, Azure), single-tenant vector stores, citation-first UX and SOC 2 posture designed into the system. No surprises at validation.
The same senior architect from the first workshop through go-live. Then we stay on: ticket triage, quarterly technology reviews, ad-hoc architecture calls.
Services
End-to-end delivery for life-sciences organisations: the visible AI work and the less visible work that keeps pharma marketing and sales running.
Dedicated LLM backends. RAG on closed knowledge bases, isolated cloud, zero external egress of trade secrets or medical data. Every generation ties back to a document ID and a retrieved passage.
Take-over of at-risk CMS estates inherited without vendor handover or documentation. Containerised local builds within days, untangled core modifications, security-update path restored.
Enterprise WordPress + WooCommerce with custom checkout, tiered pricing and region-gated content, integrated into Salesforce, Pardot, Veeva, Confluence and PubMed.
Pixel-accurate redesign implementation, cyclical campaign landing pages on Angular and Vanilla JS, custom React and Vue components: configurators, calculators, resource libraries.
Sectors we serve
A cross-section of the organisations we have delivered for over recent years.
Our products
Source-grounded content generation, a regulatory document platform and a medical-taxonomy segmentation engine, running in production for pharma and diagnostics clients. That is why we know what validation will ask before it asks.
Drafts emails, articles and social posts strictly from approved internal documents. OCR, PDF and DOC ingestion inside an isolated tenant. Every output cites the passage it came from, so hallucination risk is removed by design rather than by review.
Multi-tenant RAG over large document sets with several models behind one interface (Bedrock / Claude, OpenAI, Gemini). Modules for regulatory dossier generation, systematic literature review, medical-legal review and evidence-grid extraction.
Custom database and search engine that classifies doctors, hospitals and labs on medical taxonomy. Integrated into the storefront and CRM so segmentation is available where campaigns and deals are worked, with lead scoring on the same records.
What we built
Selected work described by the problem it solved. Client names are available on request.
Situation. Marketing and medical teams needed on-brand, source-accurate content at volume. Public LLM tools were ruled out for compliance and trade-secret reasons.
Outcome. Content teams draft from approved material only. No data leaves the tenant; every output cites its source.
Global pharmaSituation. Regulatory, medical and evidence teams spent weeks on dossiers, literature reviews and medical-legal checks across spreadsheets and PDFs.
Outcome. AI-drafted regulatory text that stays traceable to its sources, reviewed inside one tool.
PharmaSituation. Sales and marketing were segmenting customers in spreadsheets, with no shared taxonomy for doctors, hospitals and labs.
Outcome. One connected pipeline from catalog to campaign to opportunity. No side-loaded spreadsheets, no monthly manual sync.
Diagnostics & proteomics vendorsSituation. Catalogs, pricing rules and regional restrictions had outgrown template e-commerce; the storefront was disconnected from CRM and marketing automation.
Outcome. Enterprise WooCommerce integrated with Salesforce, Pardot, Veeva, Confluence and PubMed. Lead handoff without manual steps.
Lab-instrument & diagnostics vendorsSituation. Production systems inherited without vendor handover, local build or documentation. Core-CMS modifications had broken the update path.
Outcome. Containerised local builds within days. Contao, Weblication, Concrete5 and MODX estates patchable again, without a rebuild.
University children's hospital & specialty firmsSituation. In-house marketing needed successive campaign landing pages and a full redesign, on a cadence most vendors underestimate.
Outcome. Release trains that keep up with marketing. Component reuse compounds, so each campaign costs less than the last.
Plasma products & medtech componentsTechnology coverage
Full-stack technical coverage across the areas that matter for life-sciences delivery. No single-language shop.
How we work
Long-standing engagements with pharma and hospital clients have shaped a way of working that leans on senior architecture, honest scoping and continuous handoff.
From proof-of-concept through production. Architecture ownership sits with one senior engineer, the same person from the first workshop through go-live.
Accountable for scope, capacity and quality. You speak to one person and get one plan, no matter how many engineers are on it.
Source-grounding, refusal patterns for out-of-scope queries, medical-adjacent disclaimers and evaluation harnesses that track output quality across releases.
Ticket triage, quarterly technology reviews, ad-hoc architecture calls with your internal team. Zero drama, no re-selling.
Contact
Whether you are exploring an AI idea, need a legacy estate rescued or want a second opinion on architecture, we are here to help.