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Qyro

Qyro is a compliance platform for health and medtech companies, unifying quality, clinical safety, security, and AI governance in a single record. The platform covers nine standards and frameworks, including ISO 13485, DCB 0129, and DTAC, with 80+ pre-configured documents per standard. It combines AI-driven intelligence with human expert review to help suppliers get audit-ready faster and providers verify compliance continuously.

Traction –/10
HQ unknown
250+ followers
  • Regulatory & Compliance Technology
  • Healthcare Technology
  • Artificial Intelligence
  • Software Only
  • Digital Health
  • Hardware
  • Medical Devices
Updated 13 days ago

Funding

Funding rounds are not available yet.

Founders

Founder details are not available yet.

Product

Problem

Healthcare innovators developing medical devices, digital health products, and clinical solutions face fragmented quality management processes that rely on disconnected documents and manual compliance tracking. This slows product development, increases regulatory risk, and makes it difficult to maintain visibility across quality, safety, and product context as teams scale.

Solution

Qyro delivers a unified quality operating system that connects compliance work with product context, evidence, and real operational signals. The platform covers quality, clinical safety, security, and AI governance in one record, replacing disconnected documents with living artefacts that evolve alongside the product. Qyro embeds clinical safety officers, regulatory advisors, and fractional leaders directly into workflows, providing practical judgment where automation alone is insufficient. Intelligence does the heavy lifting—suggesting hazards, tracking changes, and identifying next steps—while qualified people review and decide what matters. This integrated approach transforms quality from a document-centric burden into a visible, connected system that lets suppliers get audit-ready faster and lets providers verify continuously.

Target Audience

Primary customers are health and medtech suppliers, including medical device startups, scale-ups, portfolio teams, and digital health and AI companies needing to achieve certification and secure NHS contracts, as well as providers such as NHS trusts, ICBs, and private providers that need to verify supplier compliance continuously.

Features

  • One record answering nine standards and frameworks, including ISO 13485, ISO 27001, ISO 42001, DCB 0129, DCB 0160, DTAC, DSPT, and Cyber Essentials
  • Lead libraries with 80+ pre-configured documents per standard, shaped to the company's profile rather than blank templates
  • Hazard Studio that places every hazard on the care pathway with cause, control, evidence, and owner, with intelligence suggesting likely hazards for Clinical Safety Officer review
  • Assurance Planner that reads what has changed and gives the next step, an owner, and a date to prevent audit scrambles
  • Qyro Continuum showing completeness at a glance, with evidence building as work happens
  • Learning engine that improves the system from product context, evidence, decisions, and real operational signals
This profile is AI-generated and may contain inaccuracies.