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medytrak ce marking medical consent ireland

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

crest tested medytrak eiis tax break

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.

medytrak gdpr clinical trails

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.

medytrak fda class 1 , medical consent

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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