London office · Strategy room

Healthcare app development,
clinically grounded.

Magora is a London healthcare app development company. Patient apps, clinician mobile tools and remote-monitoring apps for iOS and Android — with the FHIR, HL7 and GP Connect integration and the evidence pack an NHS buyer will ask for.

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Trusted by AstraZeneca Danone Unilever Toyota Cisco Veolia
15
Years building software in London
6
Healthcare products in the portfolio
500+
Clients since 2010
5-10
Working days to a free prototype
What we do

Healthcare apps
we ship.

Six products in this sector already, and the same pattern in each: the clinical workflow is the hard part, not the app. Building clinical systems, integrations or back-office software rather than an app? See healthcare software development.

01 — Patients

Patient apps for iOS and Android

Appointments, medication reminders, results, care plans and messaging — designed for people who are unwell, not for people testing an app.

02 — Clinicians

Clinician mobile tools

Triage, caseload, referrals, notes and handover. Built around what a working day actually looks like, with the number of taps counted.

03 — Integration

FHIR, HL7 and GP Connect

Getting data in and out of the systems already in place — EMIS, SystmOne, trust PAS — is where these projects live or die.

04 — Monitoring

Remote monitoring and wearables

Wearables, Apple HealthKit, Google Health Connect and home devices feeding an app and a clinical dashboard, with alerting rules a clinician can tune rather than a black box.

05 — Data

Reporting and analytics

Service dashboards, outcome tracking and the audit trail that has to exist before anyone will sign anything off.

06 — Evidence

The compliance pack

DTAC responses, DCB0129 hazard logs, DSPT alignment and clinical safety documentation produced alongside the build, not scrambled together afterwards.

The thing that sinks these projects

Clinical safety is not
a phase at the end.

Three things that decide whether a healthcare build reaches patients, all of which are cheaper to settle in week one than in month six.

Pillar 01

Is it a medical device?

Software that supports a diagnostic or treatment decision can fall under UK MDR and need UKCA marking — the boundary turns on intended purpose and on how the output is worded. We raise it in the first fortnight, because a product that crosses that line quietly is a product that stops at procurement.

Pillar 02

The evidence a buyer will ask for

DTAC, DCB0129 and a clinical safety officer's sign-off are not paperwork you bolt on. They shape the architecture: audit logging, data residency, role separation, failure behaviour. Built in from the start they cost little; retro-fitted they cost a re-write.

Pillar 03

Integration is the project

The app is rarely the hard part. Reading and writing a record in the systems a trust or practice already runs — and proving you did it safely — is where the weeks go. We scope that first and price it honestly.

Remote care

Telemedicine and
remote monitoring.

Two ways care leaves the clinic: apps patients use on their own phone, and dashboards clinicians work from. Both raise the medical-device question and the escalation rules early, so we settle them first.

Telemedicine

Video consultation and follow-up

Booking, secure video, in-app messaging, questionnaires before the appointment and notes and outcomes captured for the clinical record. Designed for patients on a poor connection and clinicians with ten minutes.

Remote monitoring

Wearables and home devices

Readings from Apple HealthKit, Google Health Connect, Bluetooth wearables and home monitoring kit feed a clinical dashboard. Alert thresholds are rules a clinician can see and tune, not a black box.

Safety

Alerts, escalation and failure

Who is told when a reading is out of range, what happens when a device goes quiet, and who owns the response. These go into the hazard log in the first fortnight, because monitoring that diagnoses or triggers treatment can make an app a medical device.

Before you build

Wellbeing app
or medical device?

A short test, not regulatory advice: your regulatory advisor or the MHRA makes the call. What decides it is what the app claims to do, not how it is built.

Usually a wellbeing app

Tracks and informs

Mood, sleep and habit logs, fitness tracking, appointment booking, a patient record that replaces a paper file. MHRA says monitoring general fitness, health and wellbeing is not usually considered a medical purpose.

Likely a medical device

Diagnoses, scores or advises

Symptom checkers that rank conditions, apps that assess skin from photos, tools that work out a dose or a risk score from a patient’s data. These can need UKCA marking.

Decided by wording

Intended purpose

The same app can land on either side depending on what it claims. We write the intended-purpose statement with you in week one. See four worked examples in the table on our healthcare software page, and our SaMD guide.

Process

From idea to something
a clinician will use.

The same process we run on every engagement, with the healthcare-specific questions asked early rather than discovered late.

Step 01

Clinical workflow research

1 – 2 weeks

We sit with the people who will use it — clinician, patient, administrator, carer — and map the day as it is, not as the org chart describes it. Every healthcare product we have shipped changed shape after this.

Shadowing Personas Pathway map
Step 02

Regulatory and safety scoping

1 week

Intended purpose written down, the medical-device question answered, DTAC and DCB0129 obligations identified, data flows and residency agreed. This is the fortnight that decides the next six months.

Intended purpose UK MDR check Hazard log
Step 03

Free working prototype

5 – 10 days

A running prototype of the core journey, built from your brief, before any paid engagement. Yours to keep either way — it is the fastest way to find out whether we understood you.

Clickable No commitment Yours to keep
Step 04

Integration spike

1 – 3 weeks

Before the build is priced, we prove the hard integration end to end against a real endpoint or sandbox — FHIR, HL7 v2, GP Connect, a trust PAS. An estimate that assumes the integration works is not an estimate.

FHIR R4 GP Connect Sandbox proof
Step 05

Build, in two-week slices

8 – 24 weeks

Weekly demos, a working build at the end of every sprint, and the safety documentation written as the features land rather than reconstructed from memory at the end.

Weekly demos Living hazard log Audit trail
Step 06

Handover and support

Ongoing

Source, designs and IP transfer to you on payment. We stay on for patches, framework upgrades and feature work for as long as it is useful, and hand to your team when they are ready.

Full IP transfer SLA options Clean handover
Tech stack

Technologies
we work on.

The actual stack on healthcare app engagements — native and cross-platform mobile, interoperable, auditable, and boring where boring is a virtue.

Mobile
  • Swift · SwiftUI
  • Kotlin · Compose
  • React Native
  • Flutter
Web
  • TypeScript · React
  • Next.js
  • Vue
  • Accessible by default
Backend
  • Node.js · NestJS
  • Python · FastAPI
  • PHP · Laravel
  • .NET
Interoperability
  • HL7 FHIR R4
  • HL7 v2
  • GP Connect
  • SNOMED CT · dm+d
Data
  • PostgreSQL
  • Redis
  • Encrypted at rest
  • UK data residency
Devices
  • Apple HealthKit
  • Google Health Connect
  • BLE wearables
  • Home monitoring kit
Assurance
  • DTAC responses
  • DCB0129 hazard log
  • DSPT alignment
  • UK GDPR · DPIA
AI, where it earns it
  • Triage support
  • Document summarisation
  • Coding assistance
  • Always human-in-the-loop
Selected work

Healthcare apps
we've shipped.

Six from the wider portfolio — real products, not mock-ups. Building for a pharma company? See pharma app development.

Case study

InnovoCare

Care software built with Magora — the full story, including what changed along the way.

Case study

Doctor OTC

Connecting patients with over-the-counter guidance, designed around how people actually search for help.

Case study

Medical Tourism App

Treatment abroad, from enquiry to aftercare, across providers, languages and currencies.

Case study

Healthy diet app

Nutrition tracking that people keep using past week two — the only metric that matters in this category.

Case study

BodySync

AI-drafted treatment plans for clinicians, restricted to peer-reviewed sources and built for HIPAA and GDPR. The MVP is in use in UK clinics.

Case study

Focalyx

A web application that tracks prostate cancer focal-treatment outcomes across partner clinics, with patient data and AI analysis results in one place.

Frequently asked

The honest
questions.

Is my healthcare app a medical device?
Possibly, and it is the first thing worth settling. Under UK MDR, software intended to support a diagnostic or treatment decision can be a medical device needing UKCA marking, while a wellbeing, administrative or information product usually is not. The line turns on intended purpose and on how the result is worded to the user, so it is decided by positioning long before it is decided by code. Magora is not your regulatory advisor — what we do is raise it in the first fortnight, write the intended-purpose statement with you, and build to whichever answer your advisor gives. Our guide to software as a medical device (SaMD) has examples, and the table on our healthcare software page shows four common cases.
Can you produce DTAC and DCB0129 evidence?
Yes — as the supplier side of it. We produce the technical responses a DTAC assessment asks for, maintain the hazard log through the build, and structure the system so the answers about audit logging, data residency and role separation are true rather than aspirational. DCB0129 also requires a named clinical safety officer; that is a clinical role and sits with you or with a specialist we can work alongside.
What does healthcare app development cost?
It depends on scope, and on how much integration and assurance the product needs — those two are what make healthcare cost more than the same app in another sector. We start with a free working prototype and a written analysis from a senior Product Owner, no commitment. Our 2026 pricing (GBP): Product Discovery from £3,000, a Startup MVP from £10,000, a full production web or mobile project at £25,000–£60,000. Our rates start from £49 an hour per developer, and £65–£70 an hour for a full team with QA and product ownership, and full ownership of source, designs and IP transfers to you on payment. Try the app cost calculator for a quick range.
How long does a healthcare app take to build?
A working prototype lands in 5–10 working days. A production build typically runs 8–24 weeks from kickoff, and healthcare sits at the longer end when a real integration is involved — which is why we prove the integration in a spike before quoting the build, rather than discovering it in month three.
Can a healthcare app integrate with EMIS, SystmOne or a trust system?
That depends far more on access than on engineering. The technical routes — FHIR R4, HL7 v2, GP Connect — are well travelled, and we build to them. What decides the timeline is whether you can obtain the partner agreements, sandbox access and assurance sign-off from the system supplier or the trust. We scope that honestly at the start, including the parts that are not in our gift, because an estimate that assumes access will be granted is not worth having.
Native or cross-platform for a healthcare app?
Either, and the device work usually decides it. We build native iOS in Swift and SwiftUI, native Android in Kotlin and Compose, and cross-platform in React Native or Flutter. Where an app leans heavily on Apple HealthKit, Google Health Connect or Bluetooth wearables, native often earns its cost; where it is mostly forms, messaging and content, one cross-platform codebase usually does the job. We settle it in scoping, before anything is priced.
Who owns the app code and the patient data?
You own both. Magora's terms transfer ownership of bespoke work to the client on payment, and the repository is licensed to you from the first commit. Patient data is yours throughout and stays in the UK or EU by default; we work as processor under your controllership, with a DPIA and the data-flow documentation that goes with it.
Pavel Shevtsov
About the reviewer
Co-Founder & Managing Director, Magora

Pavel co-founded Magora in 2010 and runs the company. He reviews how the teams and delivery processes described on this page are set up and run.

Reviewed 13 October 2026
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