Please find below a list of Quality Standards, Schemes and Directives for which LRQA can provide assessment, certification, verification and training services.
ISO 13485:2003 is an international standard that defines quality management system requirements for manufacturers of medical devices.
ISO 22000 is a standard which supports you in managing food safety.
The quality management system standard
This standard states the requirements for an IT service management system. This system can be used by an IT service provider to ensure an approved level of service is delivered to their customers.
HACCP
Social Accountability
The In Vitro Diagnostic (IVD) Medical Devices Directive is relevant to you if you design, manufacture or distribute IVD medical devices within the European Economic Area.
The directive covers all products which claim to have a medical purpose and which are used in and on the human body, from heart valves to scalpels, excluding in vitro diagnostics, which are covered in a separate directive.
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