Device & regulatory triage
Know your direction earlier.
Turn your device concept into a clearer regulatory starting point, with likely classifications, pathways, and sources to review.
Explore this featureAI workspace for MedTech teams
Your AI Partner for MedTech Innovation
From idea to impact. Get AI-guided clarity on every step of medical device development.
Built for non-clinical research. No patient data required.
Everything medical device development asks of you, in one place
Validate Ideas
Assess market need, competitors, and clinical value.
Design Smarter
Define requirements, explore technologies, and plan your product.
Navigate Regulations
Understand pathways, standards, and documentation.
Manage Risks
Identify hazards, analyse risks, and plan mitigations.
Plan & Execute
Get timelines, budgets, and milestones to stay on track.
Win Funding
Create investor-ready materials and go-to-market roadmaps.
How the workspace does it
Eight connected tools replace scattered notes and guesswork with one structured, collaborative workflow. It breaks down broad project goals into concrete, actionable steps allowing teams to focus on engineering and innovation rather than administrative roadblocks.
AI-Guided Conversations
Get project-aware guidance and clear, step-by-step support throughout device development.
Project Dashboard
Track project progress, milestones, tasks, health, and budgets from one calm overview.
Smart Roadmaps
Build development plans, timelines, milestones, and due dates tailored to each device.
Regulatory Roadmaps
Navigate pathways, classification, standards, verification, and documentation planning.
Risk & Compliance Book
Connect hazards, mitigations, traceability, verification, and compliance records.
Resource Library & Templates
Find regulatory guidance, proven templates, checklists, and medical device best practices.
Investor & Market Tools
Turn market evidence and competitor insights into funding materials and launch plans.
Shared Team Calendar
Coordinate tasks and milestones with live team updates, assignments, and active alerts.
Security and compliance built in from day one
Evidence-grounded AI & Inline Citations. Every generated requirement and hazard is grounded in retrieved regulatory evidence, with precise source pointers for verifiable QA review and sign-off.
Zero Shared Model Training. Your proprietary design data stays isolated in a private index for each project and is never used to train a shared global model.
Important: MedTech Copilot is built for non-clinical research and development. It is not intended for clinical decision-making or direct patient care.
SOC 2 Type II aligned
Security controls designed for audited trust.
End-to-end encryption
Data is encrypted in transit and at rest.
No PHI
Built for research and development, not patient care.
Audit logs & access control
Role-based permissions and activity visibility.
Evidence-grounded AI
Regulatory evidence and precise source pointers support verifiable QA review.
Private project intelligence
Project data stays isolated and is never used to train a shared global model.
Build with evidence. Review with confidence.
Less regulatory guesswork. Less document busywork. More room to innovate. MedTech Copilot brings regulatory direction, evidence-led drafting, and connected safety decisions into one workspace—helping your team move from concept to prototype with a clearer plan.
Curated data & sources library
780+ vetted evidence resources
Authoritative regulatory publications, peer-reviewed research, and trusted standards references—curated to ground your team's development decisions in evidence, not guesswork.
Experts on demand
Medical device development and regulatory experts
When your team needs a human second opinion, Cahir MedTech specialists in device development and regulatory strategy are available on demand—ad-hoc or through a tiered subscription.
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Evidence-grounded document drafting
Start with a draft, not a blank page.
Build focused technical documents from relevant evidence and project context, with references that make expert review more practical.
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Connected risk & compliance support
Keep safety decisions connected.
Follow risk mitigations through linked design items and verification tests, so coverage gaps stay visible as your device evolves.
Explore this featureEvidence-led decision support. Expert review remains essential and available upon ad-hoc request or through a tiered subscription feature; drafts and suggested pathways via Cahir MedTech expert guidance and review offer guarantee of regulatory clearance.
Ready to partner with Cahir MedTech Copilot on your next device?
Join early-stage MedTech teams who use MedTech Copilot to stay focused on engineering while AI keeps documentation organized.