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Clinical Trials

medyTrak delivers real-time oversight, remote onboarding, and participant management for multi-site clinical trials anywhere in the world, streamlining compliance and simplifying every step of the study lifecycle. All trial activities and data are securely recorded, providing complete visibility, global reach, traceability, and effortless regulatory reporting

  • Pillar 1: The Procedure

    • We use visual narrations to explain the nature of the treatment and its intended benefits, ensuring total clarity for the patient.

       

  • Pillar 2: The Alternatives

    • We clearly outline all available options—including clinical observation or non-surgical alternatives—facilitating a truly informed decision.

       

  • Pillar 3: The Risks

    • Inherent risks and side effects are explained transparently, managing expectations and reducing the likelihood of future disputes.

       

  • Pillar 4: Documented Comprehension

    • This is the MedyTrak difference. Patients must enter a unique on-screen code to verify they have processed the information before they can proceed

Shared Medical Consent

Homecare Management

medyTrak empowers homecare teams and families with secure visit verification, instant updates, and digital care records accessible from any device. The platform also tracks vital medical equipment and assets, ensuring transparent, reliable, and accountable care—HIQA-compliant and easy to deploy for all stakeholders

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Our software is classified as a medical device

and bears the CE mark, certifying compliance

with EU MDR 2017/745 for safety, performance, and quality

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We’re committed to safeguarding our customers’ data and maintaining the highest security standards. That’s why we recently engaged a CREST-approved cyber security firm, to conduct a thorough penetration test of our systems. This independent assessment confirms our dedication to providing a secure and trusted experience for all our users.

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We’re dedicated to protecting personal data and upholding the strictest standards of privacy and compliance. As part of our ongoing commitment, we’ve successfully achieved GDPR 2025 accreditation, demonstrating that our policies, systems, and processes meet the highest levels of data protection. This recognition reinforces our promise to keep customer information secure, transparent, and handled with utmost care.

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Medytrak  is classified as a Class I Software as a Medical Device (SaMD) under U.S. regulations and is listed with the U.S. Food and Drug Administration (FDA) as a Medical Device Data System (MDDS) in accordance with 21 CFR 880.6310. Medytrak is exempt from premarket notification requirements and is registered and listed with the FDA pursuant to 21 CFR Part 807.

PATENT PENDING
NO.63116634
PATENT PENDING
NO.63118940
ALL RIGHTS RESERVED

MediCareTags Limited

A private company limited by shares.

Registered in Ireland No 694928

Registered Office Salthill House, Salthill, Galway, Ireland.

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