Intelligence
AI that shows its evidence.
When knowledge is scattered across documents and systems, we build retrieval, extraction and agent workflows that point to their sources and stop for human approval.
Technology partner for life sciences
AI, software and cloud engineering for Pharma, Biotech, Healthcare, Medtech, Diagnostics
What we do
Most life sciences technology problems cross all three. We take responsibility for the layers your project needs, and make them work as one system.
AI that shows its evidence.
When knowledge is scattered across documents and systems, we build retrieval, extraction and agent workflows that point to their sources and stop for human approval.
Software shaped around the lab, the plant and the clinic.
When work moves between spreadsheets, inboxes and disconnected systems, we build the portals, internal tools and integrations that put status and handoffs in one place.
Cloud that is secure, reliable and ready for validation.
When scientific applications have to run every day, we provide the environments, release pipelines, monitoring and security controls that keep them dependable.
Where we help
Each starts as one bounded workflow, with the people accountable for it.
10 problems
Teams spend time locating the current version of a procedure and checking it is the approved one.
What we buildA knowledge assistant over approved SOPs and technical files that answers with references, respects document versions and flags missing evidence for review.
Collecting records for a quality or operational review is manual, repetitive and easy to leave incomplete.
What we buildAn agent that gathers material from approved systems, lists what is missing and assembles a review pack. The release decision stays with the reviewer.
Request, specimen and report status sit in separate systems, so exceptions surface late.
What we buildAn operations portal that connects available system interfaces, routes missing information and shows status and exceptions in one place.
Analyses are hard to repeat when environments, data access and versions drift between researchers.
What we buildVersion-controlled cloud environments with controlled data access, separated development and production, and repeatable releases.
Instrument exports and research records are copied by hand into the tools that analyse them.
What we buildData pipelines that collect, validate and organise laboratory outputs with lineage, then expose them to analysis and reporting applications.
Scientists cannot read everything that might matter to a programme.
What we buildClassification and summarisation of incoming publications against agreed criteria, each summary linked to its source for scientist review.
Requests arrive by email and forms, then wait for someone to decide who should act.
What we buildAn intake workflow that classifies requests, assigns an accountable owner, tracks approvals and makes exceptions visible.
Product, service and support teams lack one application connected to the platform behind the device.
What we buildA service and operations portal connected to approved device or platform interfaces through secure cloud services.
Release records, approvals and access changes are reconstructed after the fact.
What we buildVersion-controlled pipelines with security checks and least-privilege access that record what was released, when and by whom.
Teams learn about slow or failing services from their users.
What we buildAgreed reliability targets, useful dashboards, routed alerts and rehearsed recovery runbooks for the services that matter most.
How we work
Start with a focused assessment, pilot or implementation. Expand on the basis of what the work demonstrates.
Map the people, data and systems involved. Choose a bounded problem and agree what a useful result looks like.
Use representative examples to check the critical assumptions. Agree review responsibilities and acceptance criteria.
Build the application and its integrations. Test permissions, everyday use, exceptions and failure recovery.
Deploy with monitoring, documentation and a practical handover. Scope ongoing support around your operating needs.
Why Zeltar
Science informs the questions. Engineering builds the answer. These commitments shape every engagement, whatever its size.
Outputs show their sources. Quality is measured against representative cases, not the fluency of a demonstration.
Review and approval are designed into the workflow. Clinical and quality judgement stays with authorised professionals.
Intended use, data access and validation responsibilities are agreed with your quality and domain teams before the build.
Insights
Define approved sources, representative questions, evidence checks and human review before commissioning an assistant over SOPs or technical documents.
Read the guideMap one process from trigger to completion, including approvals, duplicate requests, failed updates and the person who owns each exception.
Read the guideAgree what the operating team needs to release, observe, recover and pay for an application or API after deployment.
Read the guideStart a conversation
Tell us about one workflow, application or technical challenge. Include your sector, current systems and the outcome your team needs.
Keep this first conversation high level. Please leave patient information, confidential research and sensitive documents out of the form.