Please find below a list of Quality Standards, Schemes and Directives for which LRQA can provide assessment, certification, verification and training services.
The standard which enables companies to supply to the aerospace industry. If you want to supply many of the world's largest aerospace manufacturers you will need to achieve this standard because it is now a contractual requirement for many of them.
ISO 13485 is an international standard that defines quality management system requirements for manufacturers of medical devices.
ISO 14064 is an international standard against which GHG emissions reports are voluntarily verified.
The internationally recognised quality management system standard, and the preferred solution for over half a million organisations in 159 countries.
ISO/TS 29001 provides additional requirements to quality management system standard ISO 9001 specifically intended for the petroleum, petrochemical and natural gas industries.
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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