DevOps & CI/CD for UK HealthTech — MHRA Built In
ClickMasters provides DevOps & CI/CD for UK HealthTech businesses with MHRA, NHS DTAC Domain 3 compliance from Sprint 1.
Key Highlights
Compliance
+3 more standards
Pricing
DevOps & CI/CD for HealthTech — UK Specifics
NHS DTAC Domain 3 CI/CD Requirements
DTAC Domain 3 (Technical Security): automated testing evidence, security scanning, and deployment controls. CI/CD for DTAC Domain 3: (1) automated test suite (80%+ coverage, run on every PR), (2) OWASP ZAP DAST scan on every release, (3) Trivy container scan (zero critical CVEs before deployment), (4) branch protection (two reviewers required for production merge), (5) deployment audit trail (GitHub Actions run history — who deployed, when, what changed). DTAC assessors specifically look for evidence that production deployments are controlled and tested.
NHS DSP Toolkit Standard 7 — DevOps Logging
NHS DSP Toolkit Standard 7 (Data Storage and Transmission): all access to patient personal data must be logged and retained for 6 years. DevOps implementation: CloudWatch Logs with 7-year retention configured (slightly above DSPT minimum for all-regulation compliance), CloudTrail for all AWS API activity, application-level audit log (user ID, action, patient record accessed, timestamp), and GuardDuty for anomalous access detection. ClickMasters configures DSPT Standard 7-compliant logging as standard in all NHS DevOps builds.
DCB0129 Change Management in NHS CI/CD
DCB0129 requires that software changes are assessed for clinical safety impact before deployment. CI/CD integration: (1) every pull request must include a clinical safety impact assessment (template in PR description — "does this change affect a hazard in the hazard log?"), (2) changes assessed as clinical safety relevant require CSO (Clinical Safety Officer) approval before merge, (3) all deployments to production logged with clinical safety impact assessment outcome. Audit trail: GitHub PR history serves as DCB0129 change control record — linked to hazard log.
IEC 62304 Software Maintenance and CI/CD
IEC 62304 software maintenance: changes to medical device software must go through the software change control process. CI/CD for IEC 62304: each sprint creates a new software version (IEC 62304 version increment), sprint artefacts (requirements, test reports, architecture updates) stored in Design History File (DHF). GitHub release tags link CI/CD run artefacts to DHF entries. ClickMasters configures IEC 62304-compliant CI/CD for all MHRA SaMD applications — DHF automation reduces documentation overhead by 60%.
Compliance
MHRA
NHS DTAC Domain 3
DCB0129
NHS DSP Toolkit
UK GDPR Article 9
Cyber Essentials Plus
ISO 27001
Compliance & Regulations
Every solution we build for this industry is designed to meet the following regulatory and standards requirements.
MHRA
NHS DTAC Domain 3
DCB0129
NHS DSP Toolkit
UK GDPR Article 9
Cyber Essentials Plus
ISO 27001
Investment Options
Flexible engagement models tailored to your healthtech project requirements.
£8,000–£55,000
Full engagement
- Industry-specific approach
- UK GDPR compliant
- Dedicated technical lead
£3,500–£8,000
Scoping
- Industry-specific approach
- UK GDPR compliant
- Dedicated technical lead
from £2,000/mo
Ongoing support
- Industry-specific approach
- UK GDPR compliant
- Dedicated technical lead
What Our Clients Say
Success stories from clients in healthtech industry.
“ClickMasters transformed our digital infrastructure. Their understanding of UK fintech regulations saved us months of compliance work.”
Sarah Mitchell
CTO, FinTech Solutions Ltd
“The team's expertise in NHS integrations and DTAC compliance was invaluable. They delivered on time and within budget.”
Dr. James Cooper
Medical Director, HealthFirst UK
“Their grasp of FCA requirements and insurance sector nuances helped us launch our platform 40% faster than expected.”
Michael Brooks
CEO, InsureTech Pro
Frequently Asked Questions
Common questions about healthtech software development.
What CI/CD configuration does NHS DTAC Domain 3 require?
DTAC Domain 3 CI/CD minimum requirements: automated test suite (run on every PR), security scanning (OWASP ZAP + Dependabot), branch protection (required reviews), deployment audit trail (immutable CI/CD run logs), and rollback procedure (documented and tested quarterly). ClickMasters standard GitHub Actions configuration satisfies all DTAC Domain 3 requirements and produces an evidence pack (test reports, security scan results, deployment logs) as CI/CD artefacts — ready for DTAC assessment.
Does IEC 62304 allow continuous delivery for medical device software?
Yes — IEC 62304 is compatible with agile and continuous delivery. The key: each deployment is a new software version with documented change control, clinical safety impact assessment, and test evidence. IEC 62304 does not require sequential waterfall releases — it requires that the software lifecycle process is followed for each change. ClickMasters has achieved DTAC approval and MHRA Class IIa registration for medical device software using two-week sprint cycles with continuous delivery.
Related healthtech Services
HealthTech Software Development UK — NHS-Connected, DTAC & FHIR R4
MVP Development for UK HealthTech Companies — DTAC-aware Compliant
Custom Software Development for UK HealthTech Companies — DTAC Compliant
Ready to Build for healthtech?
Let us engineer a platform that meets your industry regulations, serves your users, and scales with your ambitions.