
Dr. Olivier CRETON
Medical doctor. Brings clinical expertise and vision: science always precedes code.
Doctors and startups: we design, develop, certify. EU MDR, GDPR, French HDS — our native languages. Five medical software products in production — and the method to build yours.
Rather than describing our skills in the abstract, here are five digital medical devices we have designed, built, and certified — for doctors, clinical researchers, and industry partners.
Patient-Reported Outcome collection for vascular and phlebology surgeons. Standardized post-op questionnaires at 5 milestones (D0 → D90).
Doctor & patient platform for the multicentric study on pelvic congestion syndrome. 7 sites, 2026–2028.
MedSynApps' historic platform since 2017. Centralizes thousands of international trials to support patient inclusion.
Clinical trial data capture for CROs, investigators and sponsors. Designed to be opened by clinicians.
Remote follow-up for chronic and post-operative patients. Modular, accessible on PC, tablet, smartphone.
Congratulations on this software, it brings huge value to our patients. The feedback is consistently positive — it's a real plus in daily practice. It reassures patients and has significantly cut the number of calls to the front desk. We're staying on board!
After my varicose vein surgery, the daily messages were reassuring. Feeling that you stay in touch with your doctor without having to call for every little question — it really makes a difference. I'd recommend this kind of solution.
I really enjoyed seeing my ideas take shape in software this configurable.
We saved a lot of time setting up our investigator sites thanks to such an easy-to-use platform.
Our projects follow a proven path. At every step, you know where you stand, what is delivered, and what comes next. No regulatory surprises at the finish line.
We start from your real clinical need. No blank slate, no generic roadmap. We map usage, users, regulatory constraints, and functional scope.
Software architecture, data flows, interface design, risk management (ISO 14971), functional specifications. Whatever must be documented, is documented.
Tested, reviewed, traceable code. Modern stack (Next.js, native mobile, HDS-ready cloud). Audit trail built in from the first commit. Short sprints, regular demos.
MDR technical file, CE marking Class I or guidance toward IIa, GDPR declaration, HDS hosting, post-market vigilance. We hand you audit-ready documentation.
Deployment, monitoring, support. Corrective and evolutive maintenance under SLA. We remain your tech team for as long as you need.
Born in 2017 from the meeting between a doctor and an engineer. Eight years later, the same team still decides, codes, and writes the technical files.

Medical doctor. Brings clinical expertise and vision: science always precedes code.

Engineer. Builds the tools doctors actually want to use, within the EU MDR / GDPR / HDS framework.
Startup at prototype stage, clinician with a protocol, lab with an eCRF need: we become your end-to-end technical team — strategy, design, development, compliance, production.
EU MDR, GDPR, HDS, ISO 14971, IEC 62304: built in from the first commit. Our compliance page (in French) details our approach, MDR classes, and how we build a solid technical file.
Patient portals, back-offices, data-collection platforms. Designed for your teams, hosted in France on HDS-certified infrastructure.
Remote follow-up, ePRO collection, connected monitoring. The patient answers from their phone — you read the data when you need it.
eCRF, ePRO, recruitment, registry: structure your studies and cohorts without depending on rigid off-the-shelf tools.
TypeScript, React, Next.js, .NET, Swift, Kotlin, GraphQL: our technologies are modern because our stakes are too. Security, compliance, audit trail, HDS hosting — we don't build consumer software, we build medical software.