EU PROJECTBringing an innovative pocket-sized 12-lead ECG with AI-automated interpretation to the market: AnyECG project. CLINICAL STUDYCardiolyse Risk of Heart Disorders score predicts heart failure outcomes in the MyoVasc study DEVICE INTEGRATIONCardiolyse and MedicubeX deepen their collaboration CLINICAL PILOTPost-ablation telemonitoring with GVM Care & Research at Maria Cecilia Hospital HOSPITAL PILOTCardiolyse improves cardiovascular care at Oxford University Hospitals EU PROJECTCRANE: pre-commercial procurement for remote chronic care

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Before you write

A few things we're often asked.

How fast can we integrate the API?

Most teams reach a working proof-of-concept in about two weeks. Our REST API accepts every common ECG format and returns structured results ready to slot into your EHR, dashboard or app.

Read the API overview →

Do you support paper and PDF ECGs?

Yes. Our digitisation pipeline turns paper, PDF and photo ECGs into machine-readable signals that feed the same clinical-grade AI models used on native digital recordings.

See ECG digitisation →

Can you run a clinical trial with us?

We work with pharma sponsors and CROs on ECG endpoints — from cardiac safety monitoring to arrhythmia detection. Central reading and validation can be handled by an external clinical team.

Clinical trials & pharma →

Is Cardiolyse a certified medical device?

Yes — Cardiolyse is a CE-marked Class IIa medical device software under EU Regulations. Our quality management and information security follow ISO 13485 and ISO 27001-aligned processes.

Certifications & compliance →

Imprint

Legal entity.

Cardiolyse operates as a Finnish limited company registered in Helsinki. For contractual, invoicing or press correspondence, please use the details below.

Registered entity
Cardiolyse Oy
Business ID (Y-tunnus)
2773211-3
VAT ID
FI27732113
Registered address
Terkko Health Hub
Haartmaninkatu 4
00290 Helsinki, Finland