Overview of ISO 13485
ISO 13485:2016 is the most recognized international standard specifically developed for the manufacture of medical devices. It applies to manufacturers and organizations that support them.
The standard aims to ensure devices consistently meet customer and applicable regulatory requirements.
ISO 13485 includes the need for a risk-based approach to the quality system, enhanced focus on regulatory requirements, the responsibilities of top management, increased controls over suppliers and outsourced activities, and emphasis on risk management throughout the product lifecycle.
QMS Global Services
Certification – We provide assessment and certification to ISO 13485
Gap Analysis – We offer gap analysis and preliminary assessments to prepare you for certification
Training – QMS Global provides remote and on-site introduction and internal audit training which will prepare you and your staff prior to and after the ISO 13485 certification process