Therapeutic Area

Cardiology

Advancing cardiovascular clinical research with precision monitoring, regulatory expertise, and end-to-end Phase I–IV trial management across India.

Initiate a Cardiology Trial
Overview

Cardiovascular Trials, Precisely Managed.

Mayomi Research Solutions provides expert clinical trial management for cardiology studies ranging from early-phase safety evaluations to large-scale Phase III/IV efficacy and outcomes trials. Our team has hands-on experience across coronary artery disease, heart failure, arrhythmias, hypertension, and interventional cardiology.

We work closely with principal investigators, cardiologists, and cardiology nurses to ensure protocol compliance, accurate data capture, and regulatory alignment with CDSCO, FDA, and EMA requirements.

  • Coronary artery disease & acute coronary syndrome trials
  • Heart failure & preserved ejection fraction studies
  • Atrial fibrillation & arrhythmia management trials
  • Hypertension & lipid-lowering drug studies
  • Interventional cardiology device trials (CDSCO Class C)

At a Glance

Trial Phases Phase I, II, III, IV
Regulatory Bodies CDSCO, FDA, EMA, DCGI
Key Endpoints MACE, LVEF, QTc, NYHA Class
Patient Population Adults 18–80, high-risk CV patients
Study Types RCT, Open-label, Registry, Post-market
Location Bengaluru, Pan-India sites
Trial Capabilities

What We Deliver.

Specialized capabilities built for the unique demands of cardiovascular clinical research.

Phase I–IV Cardiac Trials

Full-spectrum trial management from first-in-human safety studies through large-scale Phase IV post-marketing surveillance and outcomes research.

ECG & Holter Monitoring

Centralised and site-level cardiac monitoring management including 12-lead ECG review, Holter interpretation support, and QTc interval tracking.

MACE Endpoint Management

Expert coordination of Major Adverse Cardiovascular Events (MACE) adjudication committees, event reporting timelines, and regulatory submissions.

Get Started

Initiate a Cardiology Trial.

Speak directly with our clinical operations team about your cardiovascular trial requirements, timelines, and site capabilities.

Contact Our Team