Seven Martin Labs designs and manufactures highly secure SaaS and SaMD (Software as a Medical Device) architectures, compliant with strict regulations, and guaranteed 100% Lighthouse performance. Proprietary code.
Free initial technical assessment. Response within 24h.
Designing intuitive, high-fidelity interfaces for health and education professionals. Clinical clarity, a11y accessibility standards (WCAG), and zero-friction operational workflows.
Robust APIs, isolated microservices, and resilient cloud-native architectures built to scale. Fault-tolerant relational DBs and secure infrastructure deployment.
Absolute compliance built-in from start: AES-256 data encryption, certified HDS / HIPAA medical hosts, GDPR compliance audits, and CE-marking technical documentation.
La précision technique et le soin du détail ne sont l'apanage d'aucun secteur. Nous travaillons avec ceux qui visent l'excellence, quelle que soit leur industrie.
Telemedicine portals, real-time patient monitoring, biomedical signal processing, and secure clinical dashboards.
Class I, II, or III diagnostic and therapeutic medical software, ISO 13485 compliant, and clinical validation ready.
Custom learning management systems (LMS), secure virtual classrooms, and AI-powered adaptive learning engines.
Complex subscription platforms, robust APIs, resilient distributed cloud architectures, and operational automation.
If your digital product demands high engineering quality and strict data compliance regulations, we build it.
We model interfaces for clinicians and students, reducing cognitive fatigue and bringing critical data front and center. React · Next.js
We engineer secure APIs supporting FHIR/HL7 biomedical standards and SCORM/LTI learning formats. Python · PostgreSQL · Node.js
HDS medical hosting, development pathways following CEI 62304 / ISO 13485 guidelines, and complete audit trail. HIPAA · HDS · ISO 13485
In health and training, every millisecond counts. Guaranteed Lighthouse 100 to ensure fast execution even on low-coverage mobile networks.
30-minute diagnostic session. We assess compliance targets (HDS, HIPAA, CE, FDA) and workflows. Deliverable: Product roadmap and fixed-price quote.
We design user interfaces and workflow screens on Figma. You validate screens and interactions before a single line of code is written.
Agile sprints with automated test coverage reports. A deployment preview environment is updated daily for review.
Verified 100 Lighthouse speed. Complete regulatory compliance file signature. Handover of proprietary code and HDS server deployment.
Developing medical-grade software or enterprise B2B SaaS demands zero tolerance for errors. Our pricing plans include rigorous testing and compliance protocols.
PROTOTYPE & VALIDATION · 3-4 WEEKS
COMPLETE SAAS PLATFORM · 6-8 WEEKS
REGULATED MEDICAL DEVICE
No slogans. Only concrete commitments — fully testable, measurable, and contractually binding in every software development protocol.
HDS (French Healthcare Hosting) and HIPAA compliance are integrated from day one or an immediate contractual penalty applies.
No sales middleman or junior project manager. You speak directly to the software architect in charge of designing and building your product.
Zero vendor lock-in. The source code, data model, and intellectual property are fully yours upon completion of payment.
Strict delivery dates written into the contract. Any delay triggers automated partial or total refunds according to defined milestones.
Absolute engineering rigor. Here are our technical answers before initiating development.
Building regulated medical devices (SaMD) or B2B SaaS requires deep engineering expertise and compliance audits (HDS, HIPAA, ISO 13485). Cheap template code leads to major data leaks and fails certification audits. We build highly valuable, compliant software assets.
You collaborate directly with a senior software engineer. No delegation to juniors, account managers, or overseas contractors. This direct connection ensures clinical-grade precision.
We follow ISO 13485 and IEC 62304 standards. Week 1: Software requirements & risk management file. Weeks 2-6: Agile code sprint under CI/CD with automated testing. Weeks 7+: Verification, validation, and CE/FDA submission file preparation.
Yes. All active production systems are backed by SLA contracts: guaranteed 4-hour response time for critical issues and continuous security telemetry.
Following a codebase audit, we can refactor systems to meet HDS data specifications, eliminate memory leaks, and optimize rendering to reach Lighthouse 100.
Describe your software requirements and regulatory target. We review specifications and respond with a technical review under 24 hours.