Careful science, close to home.

We run clinical studies, laboratory testing and genomic research in Kenya, alongside the people and institutions who will live with the results.

A 96-well plate, the workhorse of every lab we run. Twelve steps of dilution across, eight rows of samples down, and every well a person who trusted us with part of themselves.
Serial dilution Positive result Blank control

The name comes from water.Enkare Nyirobi, the place of cool water

Before it was a city, this valley was a Maasai watering place. A railway depot grew up beside the stream, the depot became a capital, and the capital became where much of East Africa now comes for medicine, research and regulation.

We started here for a plain reason. The questions that matter most about health in this region are best answered by people who live in it, who know which clinic a mother trusts, which words a consent form needs in Kiswahili, and what a community expects to hear back once the study ends.

What we do

Four connected services, so a study can move from protocol to final report without changing hands at every stage. Use one of them or all four.

Clinical research

Phase I to IV trials and observational studies, from first feasibility check to close-out. We handle the visible work, like submissions and monitoring, and the quieter work of keeping participants informed, reimbursed and well.

  • Feasibility and site selection across Kenya
  • Ethics, regulatory and research licence submissions
  • Monitoring to ICH Good Clinical Practice
  • Participant follow-up in English, Kiswahili and local languages

Laboratory diagnostics

A laboratory set up to serve both patient care and study endpoints, where every result can be traced back through the hands that touched the sample.

  • Haematology, clinical chemistry and serology
  • Molecular testing and sequencing preparation
  • Documented chain of custody from collection to result
  • Biobanking tied to the consent each person gave

Genomics and population health

African populations hold more human genetic diversity than anywhere else on earth, and they are still badly under-represented in the reference data the world relies on. We help researchers study that diversity without taking it away from the people it belongs to.

  • Cohort and sampling design for population studies
  • Community engagement before a single sample is taken
  • Data access agreements that keep governance in Kenya

Health data and biostatistics

Clean databases, analysis plans written before the data arrives, and results a regulator can audit line by line.

  • Electronic case report forms and data management
  • Statistical analysis plans and interim analyses
  • Handling personal data under Kenya's Data Protection Act, 2019

How a study runs with us

Every study is different, but the order of things rarely is. This is what working together usually looks like.

  1. Conversation

    We read your protocol and tell you honestly whether Kenya is the right place for it, and if not, why.

  2. Feasibility

    Sites, populations and recruitment estimates built from clinic records and local knowledge rather than optimism.

  3. Approvals

    Ethics committee review, Pharmacy and Poisons Board approval for trials, a NACOSTI research licence, and introductions to county health teams.

  4. Conduct

    Enrolment, monitoring and lab work, with weekly updates you can read in five minutes.

  5. Close-out and return

    Database lock and final report, then results shared back with participants and communities in words they can use.

Every sample has a name behind it, even when the label only shows a number.

Consent people understand

Consent is a conversation in the participant's own language, with time to ask questions and take the form home. If someone can't explain back what they agreed to, we haven't finished.

Data governed here

Samples and data are stored in Kenya by default. Anything that leaves the country does so under an approved material transfer agreement, for the purpose people agreed to, and nothing else.

Results that go home

When a study ends, the people who made it possible hear what was learned. We plan and budget for that from day one, so it never gets cut at the end.

We work within Kenya's research framework as it is written, not as a formality: independent ethics review, Pharmacy and Poisons Board oversight of clinical trials, research licensing through NACOSTI, and the Data Protection Act, 2019, for everything that identifies a person.

Who we work with

Our partners range from global sponsors to a single investigator with a good question and a small grant. We give both the same attention.

  • SponsorsPharmaceutical, biotech and device companies running studies in East Africa.
  • UniversitiesResearch groups who need a local lab, local sites or a local co-investigator.
  • Health departmentsCounty and national teams planning surveillance, screening and programme evaluation.
  • Foundations and NGOsFunders who want evidence their programmes work, gathered carefully and reported plainly.

Questions people ask us

If yours isn't here, ask it directly. We'd rather answer early than discover a problem halfway through.

Can you work with sponsors based outside Kenya?

Yes, and most of our sponsors are. We act as your team on the ground: we handle local submissions, contracts with sites, and day-to-day conduct, and report to you on whatever schedule your study needs.

How early should we get in touch?

Ideally before the protocol is final. A short conversation at the design stage can save months later, especially on recruitment targets, visit schedules and sample handling.

Which languages do you use for consent?

English and Kiswahili as standard, and local languages wherever a study population needs them. Translations are checked by back-translation and tested with people from the community before use.

Where are samples stored, and can they be exported?

Samples are stored in Kenya by default. Export is possible where the study requires it, under an approved material transfer agreement and only within the scope participants consented to.

Do you take on small, investigator-led studies?

We do. Some of the most useful work we see starts with one person and a modest budget. Tell us what you have and we'll tell you what's realistic.

Tell us what you're working on.

A single page is enough to start. We'll come back with an honest view on feasibility, including when the answer is that Kenya isn't the right fit.

Nairobi, Kenya

  • The questionWhat you want to learn, in a sentence or two.
  • The populationWho you hope to enrol, and roughly how many.
  • The timelineWhen you'd like to start, and any dates you can't move.
  • The stage you're atAn idea, a draft protocol or a funded study ready to go.