Certification

Once a successful assessment is carried out and technical approval given, we award you a certificate. It provides credibility for your stakeholders through the globally recognized LRQA brand.

LRQA has offered independent, impartial assessment and certification since 1985, and many of the world’s leading companies choose us for their Business Assurance needs. Why? The answer is simple.  With LRQA, your assessors are industry experts and specialists – matched with your business needs – and trained to deliver effective and robust assessments of your systems and processes, ensuring they compliment and help you achieve your business goals and objectives. 

And, you have the confidence that our Business Assurance approach ensures our assessments focus on the areas and issues that are important to your business, helping you improve performance and reduce risk.

Quality

Accoredon banner - Quality

ISO 13485 Medical Devices

LRQA provides accredited certification and training services to ISO 13485, the quality management system requirement for manufacturers of medical devices.

TL 9000 telecom quality management

TL 9000 was developed in 1998 by QuEST Forum to meet the quality requirements of the telecommunications industry supply chain. TL 9000 is an extension of ISO 9001:2008 and organizations are expected to comply fully with ISO 9001.

Aerospace

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AS9100, AS9110 and AS9120

Based on ISO 9001, LRQA can provide certification to AS9100 which places greater emphasis on safety, reliability and compliance for the aerospace industry.

Automotive

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Automotive Standards

IATF 16949:2016 Automotive

In October 2016, the International Automotive Task Force (IATF) published a revised quality management system (QMS) standard specifically for the automotive industry, known as IATF 16949:2016.

Environmental and Energy

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Standards we Certify

CARB Verification services

The California Air Resources Board, also referred to as CARB or ARB, is the agency responsible for air quality in the California state government. If your company or facility is required to have to your greenhouse gas (GHG) emissions verified under the California Global Warming Solutions Act of 2006 (AB32), LRQA can help with our accredited ARB verification services.

CDP Recognized Standards

Is an independent not-for-profit organization holding the largest database of primary corporate climate change information in the world.

Corporate sustainability reporting

Corporate Sustainability Reporting, alternatively known as CSR reporting, is the process whereby companies - public, private; large and small - report on their non-financial performance. These reports allow organizations to demonstrate to stakeholders the impact their activities are having on the environment, society and sustainability.

ISO 14001

Certification to ISO 14001 from LR will help drive the efficient use of raw materials and therefore reduce costs to your business.

ISO 14064 verification

LRQA delivers verification and training services to ISO 14064 to help you provide credibility and assurance to support your organizations GHG emission claims.

ISO 26000 Gap Analysis – Social responsibility

LRQA can provide a Gap Analysis against ISO 26000, a guidance document to help you identify the principles and core subjects that your organization should be managing to ensure societal risks and impacts are kept to a minimum.

ISO 50001

ISO 50001 is an international standard developed by the International Organisation for Standardisation (ISO) which provides organisations with the requirements for energy management systems. ISO estimates that the standard could influence up to 60% of the world’s energy use.

MRV Regulation (EU) 2015/757

The objective of the MRV Regulation is to develop a better understanding of fuel consumption and CO2 emissions from shipping activities within the EU which could then be used to shape and inform any future GHG monitoring or reduction initiatives. The MRV Regulation is viewed as the first step of a staged approach for the inclusion of maritime transport emissions into the EU’s GHG reduction commitment, alongside the other sectors that are already contributing to that commitment.

Health & Safety

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Corporate sustainability reporting

Corporate Sustainability Reporting, alternatively known as CSR reporting, is the process whereby companies - public, private; large and small - report on their non-financial performance. These reports allow organizations to demonstrate to stakeholders the impact their activities are having on the environment, society and sustainability.

ISO 26000 Gap Analysis – Social responsibility

LRQA can provide a Gap Analysis against ISO 26000, a guidance document to help you identify the principles and core subjects that your organization should be managing to ensure societal risks and impacts are kept to a minimum.

ISO 45001

ISO 45001 is the world’s first international standard for occupational health and safety (OH&S) management developed to be applicable to any organization regardless of its size, industry or location.

OHSAS 18001

OHSAS 18001 has been developed in response to industry demand for a recognisable health and safety management system standard which can be externally assessed and certified.

Food Safety

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BRC Global Standard for Food Safety Issue 8

The BRC Global Standard for Food Safety was first published in 1998 and released on August 1, 2018 in its 8th issue. The standard provides a framework to manage product safety, integrity, legality and quality for the food manufacturing, processing and packing industry.

BRC Global Standards

BRC Global Standards and Schemes are used by suppliers and global retailers. They facilitate standardization of quality, safety, operational criteria and manufacturers’ fulfillment of legal obligations. They also help provide protection to the consumer.

DNA1 Consumer Assurance

DNA1 consumer assurance from Lloyd's Register and Clear Labs delivers protection for your brand and your consumers.

Food Safety Modernization Act (FSMA) Services

The FDA Food Safety Modernization Act (FSMA) was signed into law by President Obama on January 4, 2011. It aims to ensure the U.S. food supply is safe by shifting the focus of federal regulators from responding to contamination to preventing it.

Foreign Supplier Verification Service to Support FSMA requirements

The US FDA issued FSMA Final Rule on Foreign Supplier Verification Programs (FSVP) for Importers of Food for Human and Animals is now final. For the purposes of FSVP, an importer is the U.S. owner or consignee of a food offered for import into the United States. How are you ensuring your suppliers are in compliance? LRQA’s foreign supplier verification services can evaluate hazard- and risk specific criteria.

FSMA Accredited Foreign Supplier Facility Certification

To support this requirement, the FDA FSMA rule on Accredited Third-Party Certification has been finalized, and the program is now open for participation. The rule establishes a voluntary program for the accreditation of third-party certification bodies, like Lloyd’s Register (LR), to conduct food safety audits and issue certifications of foreign entities, including farms, and the foods for humans and animals they produce section 806(d) of FSMA. LR is working towards FDA-recognized accreditation to deliver food safety audits and Accredited Third-Party Certification under FSMA.

Medical Devices

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In-Vitro Diagnostic Directive - New EU IVDR

The In-Vitro Diagnostic (IVD) Device Regulation is approaching the final stages of the review process before becoming law and is the proposed revision to the existing IVD Directive 98/79/EC.

ISO 13485 Medical Devices

LRQA provides accredited certification and training services to ISO 13485, the quality management system requirement for manufacturers of medical devices.

MDD 93/42/EEC Medical devices

We’re designated as a notified body under the medical devices directive for medical devices using the quality system conformity routes laid out in Annexes II, V and VI.

MDSAP - Medical Device Single Audit Program Certification

Recognizing that a global approach to assuring the safety of medical device manufacturing would provide tremendous benefit to the industry and the end user, the International Medical Device Regulators Forum (IMDRF) has created a harmonized approach to auditing and monitoring the manufacturing of medical devices.

Medical Devices Directive - New Regulation

As with the upcoming In-Vitro Diagnostic (IVD) Device Regulation, the proposed Medical Device Regulation (MDR) is also approaching the final stages of development before becoming law as a Regulation.

Information Security

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ISO 27001 certification

ISO 27001 certification with LRQA ensures you have the controls in place to protect your information from fraud, cyber attack, sabotage and viruses.

Managed Security Services

Learn about our managed cyber security services, including threat intelligence, security operations center (SOC) and security as a service - from Nettitude, a member of Lloyd's Register

PCI Compliance, Audit & Certification

PCI DSS compliance, certification and security service (including PCI DSS 3.2) as a qualified security assessor (QSA) - request a PCI audit today from Nettitude, a member of Lloyd's Register

Penetration Testing

Learn about our penetration testing (pen testing / pentest) security and vulnerability management services - request a vulnerability assessment today from Nettitude, a member of Lloyd's Register

TL 9000 telecom quality management

TL 9000 was developed in 1998 by QuEST Forum to meet the quality requirements of the telecommunications industry supply chain. TL 9000 is an extension of ISO 9001:2008 and organizations are expected to comply fully with ISO 9001.

Supply Chain Security

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ISO 28000

ISO 28000 is an international standard for security management systems for the supply chain. It is suitable for all sizes and types of organizations including service industries, transportation, energy, manufacturing and marine.

Business Improvement

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ISO 22301 Business continuity

ISO 22301 specifies requirements for setting up and managing an effective Business Continuity Management System (BCMS). It is auditable, enabling organizations to demonstrate compliance.