MedTech + commercial app development

Rapid mobile app prototypes and minimum viable products.

JonWard Studios designs and develops mobile apps for MedTech and commercial teams.

The goal is to put the expected workflow on a device early, test it, and give the team a working build for review, demonstrations, or an investor meeting before a larger development investment.

Discuss an app

Choose the build level

A prototype and a minimum viable product (MVP) serve different milestones.

A prototype is a simpler design and build centered on the primary workflow. An MVP connects the agreed core workflows for customer or beta use.

01 / Prototype5 business days · target

Test the primary workflow.

A working proof of concept for workflow testing, internal review, demonstrations, or investor meetings.

  • Primary app workflow from start to finish
  • Working mobile prototype
  • Concept and workflow testing
  • Internal review, demonstrations, or investor meetings
02 / MVP15 business days · target

Use the agreed core workflows.

A broader working build for evaluation, testing, demonstrations, or fundraising.

  • Agreed core workflows connected in one app
  • Working mobile MVP
  • Customer or beta use
  • Evaluation, testing, demonstrations, or fundraising

Client review and testing builds are provided through Apple TestFlight. Delivery targets begin after the scope and required project inputs are agreed.

Included with the build

Working software, testing, and project records.

Every project includes a design and development file. Its contents reflect the product and agreed build scope.

01

App design and development

Screens, interactions, requirements, and working software for the agreed workflow.

02

Design and development file

Agreed requirements, design, risks, traceability, testing, and release records.

03

Baseline usability file

Usability records covering the workflow, use environment, and evaluation findings.

04

Source handoff

Source repository and project files for the completed build.

MedTech projects

Add the regulatory baseline.

MedTech work also includes a regulatory strategy and usability engineering file.

The early-stage work follows applicable FDA guidance for device software and cybersecurity and relevant ISO 13485 design and development requirements. The resulting records can be carried into future development and premarket submission work.

MedTech app development

A direct development path

Define. Design. Build. Hand off.

01

Define

Confirm the intended user, expected workflow, milestone, and required inputs.

02

Design

Map the screens, interactions, data, and requirements for the agreed build.

03

Build

Develop and test the working app while producing its project records.

04

Hand off

Complete the final review and receive the source repository and project files.

Start with the concept

Tell us what you want the app to do.

Share the intended user, expected workflow, near-term milestone, and what the prototype or MVP needs to demonstrate.

Contact Jon