Turntiles
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Doctor interacting with holographic human body
What We Do

Services built for scaling MedTech.

Six core service capability offerings designed to eliminate technical debt, ensure regulatory compliance, and support international commercialization.

01

Discovery Workshops

Validate your software architecture, regulatory strategy, and NHS/EU clinical data pathways before writing a single line of production code.

  • ✔ Architectural assessments & diagrams
  • ✔ Integration maps (EHR, QMS, Patient Portals)
  • ✔ Feasibility & security risk assessments
Discovery Workshop
Product Development
02

Product Development

Full-stack engineering teams using automated pipelines to ship IEC 62304 compliant backend APIs, client portals, and desktop/mobile applications.

  • ✔ React, Node.js, Python, and Go stacks
  • ✔ Clinically-validated UX/UI layout designs
  • ✔ Automated continuous testing & validation logs
03

Integrations

Establish safe communication between your core software, electronic health records (EHRs), lab databases, and quality management tools.

  • ✔ HL7 FHIR and custom REST/gRPC wrappers
  • ✔ Epic Systems, Cerner, and NHS integration routes
  • ✔ QMS integrations (Greenlight Guru, Qualio)
Integrations
Infrastructure & Security
04

Infrastructure & Security

Host medical data securely on AWS, GCP, or Azure with end-to-end data encryption, automated backups, access controls, and logging.

  • ✔ HIPAA and GDPR-compliant databases
  • ✔ NHS Digital Health DSPT-aligned infrastructure
  • ✔ 24/7 Security Operations Center integration options
05

MVP & Vibecoding Rescue

If your prototype is failing due diligence or cannot pass clinical quality audits, we review the code and rebuild what is needed to stabilize it.

  • ✔ Comprehensive architectural reviews
  • ✔ Clean, testable, fully documented refactoring
  • ✔ Transition to a robust production infrastructure
MVP Rescue
Maintenance & Growth
06

Maintenance & Growth

We provide continuous feature iteration, bug resolutions, performance optimization, and regular security patches for your medical software.

  • ✔ Continuous compliance monitoring
  • ✔ SLA-backed support response times
  • ✔ User feedback & telemetry collection systems
Cost & Time Savings

Calculate your compliance savings

Software design controls and traceability mapping can consume up to 40% of a development team's engineering hours in regulated environments.

Slide the controls to select your target medical device risk classification and engineering team size to see how much time and expense Turntiles can save you.

*Estimates based on typical IEC 62304 and ISO 13485 audit prep cycles.
8 Developers
Trace Matrix Dev Hours Saved
Per launch cycle
384 hrs
Time-to-Market Acceleration
Audit readiness speedup
2.5 months
Estimated Cost Savings
In compliance engineering overhead
$34,500
Ecosystem

Validated technology stacks we leverage

Backend Systems

  • Python (Django, FastAPI)
  • Go (Golang)
  • Node.js

Frontend & Apps

  • React & Next.js
  • TypeScript
  • Flutter (Mobile)

Databases & Cache

  • PostgreSQL (RDS / Cloud SQL)
  • Redis
  • DynamoDB

DevOps & Cloud

  • AWS / GCP
  • Terraform
  • Kubernetes & Docker
Engagement

How we partner with MedTech teams

Dedicated compliance pods

A full engineering team consisting of senior developers, a solutions architect, and a QA manager working exclusively on your product under ISO 13485 controls.

Discovery & Architecture sprints

A focused, fixed-scope 2 to 4-week engagement to validate technology frameworks, map regulatory requirements, and draft initial design logs.