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Over half of the world's top 200 companies choose LRQA for certification.

LRQA is a leader in certification of the medical sector working with leading medical device and healthcare organizations. We hold approved notified body status for directives 92/42/EEC and 98/79/EC which require products to be independently examined and approved.

LRQA assessors are industry experts and specialists who are matched with your business needs, enabling an effective and robust audit of your system.

As an organization who understands the medical device industry, we offer the following services to help meet your needs:

• ISO 13485 Medical Devices
• ISO 13485 under the CMDCAS program
• 93/42/EEC Medical Device Directive
• 98/79/EC IVD Directive
• ISO 9001 Management Systems
• ISO 14001 environmental management
• Quality, environment, health and safety and information security training courses
• Integrated assessments
• Corporate report verification
  

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