LRQA Singapore - measure the differenceLRQA Singapore - measure the difference

Environmental

Environmental Standards, Schemes and Directives

Standards, Schemes and Directives

Please find below a list of Environmental Standards, Schemes and Directives for which LRQA can provide assessment, certification, verification and training services.

Standards

  • ISO 14001

    ISO 14001 is the international specification for an environmental quality management system (EMS).

  • ISO 14064

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

  • ISO 9001

    The quality management system standard

  

Schemes

  • Corporate Reporting

    Corporate Reporting is a process which evaluates a company's 'sustainability'

  • 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.

  • TL 9000

    TL 9000 defines quality management system requirements for the telecommunications industry.

  • ISO/TS 16949

    TS 16949 applies to the design/development, production and, when relevant, installation and servicing of automotive-related products.

  • BRC Standard - Food

    Approval to the BRC global standard - food gives significant benefits to the supplier. It helps to avoid the confusion and disruption that multiple audits can bring and the need to duplicate variations on the same data for different clients

  • BRC/IOP global food packaging standard

    Manufacturers have an obligation to put appropriate systems and controls in place to ensure the suitability of their packaging for safe food use

  • Clean Development Mechanism

    We will make flexible arrangements with all parties involved to make sure your project design documents and other key documents are independently validated and your actual emission reductions are verified against scheme requirements

  

Directives

  • 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.