Clinical-stage biotech, pharmaceutical, and medical practice sites built by people who read the source material before writing a word. Pipelines, trial information, investor pages, and patient-facing content—handled carefully, in English and French, with PhD-level scientific writing available.
A roofing company can tolerate a loose sentence on its website. A clinical-stage company cannot. Your copy is read by investors comparing you to three competitors, by clinicians deciding whether to refer a patient, and by patients or families trying to understand whether a trial applies to them.
That means the writing has to be precise, the structure has to make a complicated pipeline legible at a glance, and nothing goes live until the person responsible for accuracy has signed off on it. We build to that standard—the same care we put into custom software, applied to content where a wrong word has consequences.
We are a web and software shop, not a regulatory consultancy. We build the site and the workflow around your review process; your medical, legal, and regulatory people approve what it says. That division of labour is deliberate, and we will tell you plainly where our work stops.
From a single clinic site to a full corporate presence for a company heading into trials.
The full corporate presence: science, mechanism of action, pipeline by phase, team and publications. Structured so a visitor understands what you do in thirty seconds and can go three levels deeper if they want to.
A pipeline is a table with a lot riding on it. We build it so phases, indications, and status stay readable on a phone, and so updating a program after a milestone takes minutes rather than a developer ticket.
Press releases, publications, presentations and news tickers that you control. Announcement day should not require an email to your web company—you post it yourself, and it is live.
Plain-language pages for patients, caregivers, and referring clinicians: what the trial is, who qualifies, where the sites are, and how to ask a question. Written to be understood, not to impress.
For dietitians, chiropractors, clinics and private practices: transparent rates, an FAQ that answers the questions people actually call to ask, and online booking that fills the schedule without a receptionist relaying it.
Custom software that mirrors how your organization actually signs things off: draft, internal review, approval, publish—with a record of who approved what and when. We have built this kind of multi-stage review system before.
PhD-level scientific writing is available for this work—investor pitch decks, website wording, and the plain-language patient copy that still has to hold up when a clinician reads it closely. Writing that starts from your data and your publications rather than from a template, and that knows the difference between a claim you can make and one you can't.
Real projects, live today.
Clinical-stage biotech. Pipeline, technology and trial information presented for three different audiences at once—patients, clinicians and investors—with a news ticker the team updates themselves.
A company built on one targeted mechanism across several neuropsychiatric indications. The site had to make that story land quickly for investors while holding up to scrutiny from clinicians.
Bilingual dietitian practice. Transparent rates, an FAQ that pre-answers the objections that used to come by phone, and online booking.
Those are the moments a site stops being cosmetic. Let's talk before the deadline, not after it.
We go through your publications, deck, and existing material before proposing structure. You should not have to teach us your mechanism from scratch.
We map the site around your audiences and decide what belongs on the surface versus one click down. This is where most sector sites go wrong.
We write, you review. Nothing goes live until the person accountable for accuracy has approved the wording.
You get a CMS for the parts that change—news, publications, pipeline status—so routine updates never wait on us.
We are a hand-coding web and software shop with nineteen years of work behind us, and clients in clinical-stage biotech, pharmaceuticals, and private practice. We build the site, write the first draft—with PhD-level scientific writing available when the material calls for it—and build the workflow your team reviews it through.
We are not a regulatory or medical-affairs consultancy. We do not approve claims, write regulatory submissions, or certify a site as compliant with any particular framework. If your project requires that, you need those specialists alongside us—and we will work to their sign-off rather than around it. If you need hosting arrangements or data handling to meet a specific standard, tell us early and we will tell you honestly whether we can meet it.
Whether you're a two-person clinic or a company preparing for Phase 2—tell us what you need it to do, and we'll tell you straight what it will take.