LRQA Thailand - measure the differenceLRQA Thailand - measure the difference

Validation and verification

Validation and verification

Validation is a service which is related to climate change schemes introduced by the Kyoto protocol.

We offer validation of project design and other required documentation for Clean Development Mechanism (CDM) or Joint Implementation (JI) projects. This is essential for the project to be registered.

For more information about CDM and JI projects, visit the project information or greenhouse gases schemes areas by following the links below.

An LRQA verification assures your company's reported data and information. The verification should confirm that your data and information is accurate and that the data management system provides the infrastructure to collect and analyse the data and information used by decision makers such as stakeholders, regulators and your own company.

For more information about LRQA's verification services, use the links below. Alternatively get in touch with your nearest LRQA representative by using our contact finder.

Standards we validate

  • Eco-Management and Audit Scheme (EMAS)

    The Eco-Management and Audit Scheme (EMAS), is a voluntary EU directive designed to improve a company's environmental performance.

  • Greenhouse gas emissions

    LRQA work with organisations to help them demonstrate their emission reductions and compliance with national requirements.

  • ISO 14064

    ISO 14064 is an international standard against which GHG emissions reports are voluntarily verified.

  • HACCP

    HACCP

  • SA 8000

    Social Accountability

  • In Vitro Diagnostic Medical Devices Directive

    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.

  • Medical Devices Directive

    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.