Ackomas is a company specialized in data management and analysis applied to the medical device, pharmaceutical and wine & spirits industries


Four complementary forms of expertise, one solution, perfect knowledge of traceability, unit identification and regulations

The solution

A powerful tool capable of managing regulatory requirements centrally for the pharmaceutical and medical device sectors. Registering Basic UDI and UDI-DI data, synchronisation with Eudamed, batch traceability tracking, etc.


The KOA solution developed by Ackomas applies to a wide range of sectors in which traceability is key.


The Ackomas search engine provides quick access to regulations by medical device, industry and geographical target area.


Find all our news here, along with useful information about medical devices and current regulations.

Ackomas and Nexialist co-present a webinar focusing on Eudamed

Nexialist organized a webinar dedicated to Eudamed, the European medical device database. The implementation of European regulations EU2017/745 MDR and EU2017/746 IVDR continues to raise questions for medical device manufacturers. For this reason, Nexialist, the consulting firm specializing in regulatory intelligence and compliance for healthcare products, recently organized a webinar on the subject and invited…


Published in DeviceMed France

Published at the beginning of September, DeviceMed France's latest issue looks at Eudamed compliance, the means to achieve it and the urgent need to implement suitable tools, featuring KOA software, a SaaS solution developed by Ackomas. Happy reading! Download the article


Eudamed registration, creation of the Master UDI-DI

European regulations require a unique identification system for medical devices (UDI) to improve and facilitate traceability. After launching a major consultation process last spring, the European Commission has just approved the creation of a Master UDI-DI for certain so-called "highly individualized" medical devices. The medical devices, such as contact lenses, which were included in the…


Webinar – Practical questions about Eudamed compliance

The timetable for the implementation of regulations EU 2017/745 and EU 2017/746 continues to unfold, with an important next step: the operational qualification of the EUDAMED database. This step, which makes mandatory the publication of data on Medical Devices and In Vitro Diagnostics, still raises many questions among industry professionals. Ackomas is organizing a webinar…


Ackomas participates at Medi’nov Connection

On May 1st and June 1st, Ackomas will exhibit at the Medi'nov Connection 2023 which will take place at the Lyon Convention Center. Medi'nov Connection is one of the world's leading events in medical innovation and has become a must-attend event for all actors in the field of health technologies. On this occasion, Stéphane Ancel,…


Stéphane Ancel new Sales Director at Ackomas

Ackomas, a French company that specialises in publishing SaaS solutions for medical devices, is strengthening its leading position by welcoming Stéphane Ancel as Sales Director. He will be responsible for accelerating growth in the SME, mid-cap and key account segments in the MD industry. This sector is facing growing pressure with the implementation of Regulation…