Looking for an eQMS for ISO 13485 certification
NORBIT’s key requirements for an eQMS included compatibility with their existing in-house system, ease of use, and the ability to improve the efficiency of their internal processes. On top of this, they had set themselves an ambitious deadline by which to achieve ISO 13485 certification.
MedQdoc proved to be the ideal choice of eQMS and was easily adopted by NORBIT’s team, enabling them to put robust internal processes and documentation in place to support the certification.
I would absolutely recommend MedQdoc to other companies in the medical device world. Without a doubt, using MedQdoc has been a key factor in the success of our ISO 13485 certification process.
Kristian Nisja, QA & HSE Manager, NORBIT EMS Selbu
What is ISO 13485?
ISO 13485 is an internationally-agreed quality management system standard for organisations involved in the design, production, installation and servicing of medical devices. ISO 13485 certification, carried out by an independent third party certification agency, demonstrates that an organisation’s quality management system has met the requirements of this standard, thereby complying with the Medical Device Regulation.