Ackomas

Ackomas – Your Trusted Partner in Global Medical Device Compliance Ackomas empowers medical device manufacturers, regulatory teams, and compliance professionals with automated solutions to streamline regulatory processes across multiple jurisdictions. Our cutting-edge SaaS platform ensures seamless compliance with key regulatory databases, including: EUDAMED (Europe) SWISSDAMED (Switzerland) GUDID (USA – FDA) SFDA (Saudi Arabia) MHRA (UK) TGA (Australia) NMPA (China) Why Choose Ackomas? Automated UDI Management – Direct integration with global regulatory databases Real-Time Data Synchronization – Stay compliant with evolving regulations Intuitive & Scalable Platform – Designed for seamless adoption by teams of all sizes Guaranteed Compliance – MDR, IVDR, FDA 21 CFR Part 820, and ISO 13485 ready From UDI registration to audit readiness, we help you achieve full compliance with confidence! Let’s simplify compliance together! Contact us today: ackomas.com