To maintain ImmunoDiagnostics' high standards, quality should be optimised to fulfil customer needs and expectations.
Our Quality Management System ensures customer requirements are met and guarantees compliance with national and regional laws, regulations and standards.
The high quality of our products is secured through our Quality Management System. This established system outlines the policies and procedures necessary to improve and control various processes, ultimately leading to improved business performance.
The Quality Management System ensures compliance with national and regional regulations:
- European Union Directive: 98/79/EC, In Vitro Diagnostics Directive – IVDD
- USA FDA: 21 CFR Part 820, Quality Systems Regulation
Current Good Manufacturing Practices for Medical Devices & In Vitro Diagnostic Products:
- ISO 13485:2003 (including requirements related to the Canadian Medical Device Regulations, CMDR)
- ISO 14971:2009 Risk Management
Download ISO certificates for reference