ISO 13485

ISO 13485: DBM Medix's certified regulatory expertise

Quality assurance in accordance with ISO 13485

Choosing DBM Medix for your microfluidic needs means choosing a partner deeply committed to quality assurance. With this in mind, we are pleased to announce that we are in the process of obtaining ISO 13485 certification.

A benchmark for medical device manufacturers and associated service providers in terms of process management, traceability and documentation, it reflects our vision of the industry and the quality we aim to deliver.

By adhering to it, we commit ourselves not only to meeting regulatory requirements, but also to demonstrating an unwavering commitment to the production and marketing of microfluidic solutions, prioritizing safety, reliability and compliance.

Just a little more patience: our certificate will be available by the end of 2024.