INDUSTRY
Healthcare AI
Clinical expertise meets engineering precision.
Healthcare and MedTech organisations operate at the intersection of clinical urgency and regulatory rigour. Every process - from device manufacture to patient-facing diagnostics - must be traceable, validated, and audit-ready. Yet many health systems still depend on paper-based workflows, siloed clinical databases, and manual quality checks that cannot scale with growing patient volumes or tightening compliance requirements.
Medical device manufacturers face a parallel challenge: EU MDR and IVDR regulations demand comprehensive technical documentation, post-market surveillance, and validated production processes. The cost of non-compliance is not just financial - it can mean delayed product launches, market withdrawal, or patient harm.
Tavlo brings disciplined engineering to healthcare AI. We build solutions that respect the regulatory landscape - GxP, CE Marking, ISO 13485, HIPAA, GDPR - while delivering measurable improvements in clinical operations, documentation pipelines, and quality assurance.
Use Cases
Clinical Operations Optimisation
Analyse patient flow, resource utilisation, and scheduling data to reduce wait times and improve throughput across departments.
Audit-ready Documentation Pipelines
Automate the generation, versioning, and validation of technical files, DHFs, and post-market surveillance reports for regulatory submissions.
Document Compliance for Regulatory Submissions
Extract, cross-reference, and validate data across clinical evaluation reports, risk management files, and design dossiers.
Visual Quality Inspection for Medical Device Manufacture
Deploy camera-based inspection systems on production lines to detect micro-defects on implants, instruments, and packaging.
Predictive Maintenance for Medical Equipment
Monitor imaging systems, lab analysers, and surgical robots to predict component failures and avoid unplanned clinical downtime.
AI Knowledge Assistants for Clinical Teams
Retrieval-augmented generation systems that surface relevant protocols, drug interactions, and guideline updates in natural language.
Standards
Common questions
What healthcare AI solutions does Tavlo deliver?
Clinical operations optimisation, audit-ready documentation pipelines, document compliance for regulatory submissions, visual quality inspection for medical device manufacture, predictive maintenance for medical equipment, and AI knowledge assistants for clinical teams.
Does Tavlo understand EU MDR and IVDR requirements?
Yes. We build solutions that respect the regulatory landscape - GxP, CE marking under MDR and IVDR, ISO 13485, ISO 14971, HIPAA and GDPR - and we automate the technical files, design history files and post-market surveillance reports those regulations demand.
How does Tavlo handle traceability and audits in clinical settings?
Every process we build is designed to be traceable, validated and audit-ready. Our AI knowledge systems include provenance tracking, citation of source documents, role-based access control and full audit logging - because in regulated care, knowing where an answer came from matters as much as the answer.
Does Tavlo have its own healthcare product?
Yes - WoundAssist, AI-assisted wound documentation for professional care teams in the DACH region, currently in clinical pilot preparation. Every AI-assisted assessment is verified by a qualified professional; it is not yet CE-marked as a medical device.
How do we start a project with Tavlo?
Write to contact@tavlo.tech and describe the process or line you want to improve. We respond within two business days and typically start with a 30-minute call. There is no public price list - engagements begin with a conversation, and implementation details are shared under NDA.
Your next intelligent system starts here.
Whether you're in DACH or beyond, we're ready to deliver.