Efor and Ackomas elevate partnership to support medical device compliance
4/09/2025
Efor, a global engineering compliance consultancy, and Ackomas, a software solutions expert in regulatory compliance for medical devices, are taking their partnership to a new level. This collaboration, first established in 2024, addresses the growing regulatory complexities faced by medical device manufacturers across Europe and beyond.
A historic partnership
The alliance between Efor and Ackomas was forged to address the growing complexity of European Union regulations, especially concerning EUDAMED—the centralized database designed to improve the monitoring, traceability, and transparency of medical devices. While Ackomas provides an innovative digital solution that enables rapid and efficient uploads of Unique Device Identifiers (UDI), Efor offers hands-on support at every stage of a project, guiding clients through regulatory compliance challenges. Clients can lean on Ackomas’ proven software solutions and the consulting strength of Efor to navigate the complexities of regulatory compliance with confidence.
Over the past year, this robust partnership has enabled both companies to provide comprehensive support to a wide range of medical device manufacturers, ensuring compliance with EU regulations (2017/745 and 2017/746) and fostering a safer, more transparent healthcare environment.
A strengthened collaboration
This September marks a new chapter in the Efor x Ackomas partnership. While the foundation of the collaboration remains rooted in regulatory excellence and client-focused solutions, the enhanced partnership comes with a refined service offering.
The joint initiative now offers tiered licensing packages to suit clients’ varied needs, with exclusive discounts available via Efor. Additionally, the partnership is expanding its support for multi-regulatory integration—covering not only EUDAMED but also other databases like GUDID (USA), SWISSDAMED (Switzerland), NHRA (Bahrain), and SFDA (Saudi Arabia).
“This evolution to our partnership reflects both our commitment to meeting the needs of our clients and our readiness to adapt to the changing regulatory environment,” said Julie MARION, Co-founder of Efor Group and Head of Strategy & Operations. “Together with Ackomas, we ensure that medical device manufacturers can transition effortlessly into compliance mode, while also securing long-term operational efficiency.”
For more details on the Efor x Ackomas partnership and the exclusive service packages available, contact us.
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