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Training – Medical Devices

ISO 13485 identifies the requirements for a quality management system to be used by an organization involved in one or more stages of the life-cycle of medical devices. This can include the following:-
  • Design and Development
  • Production
  • Storage and Distribution
  • Installation
  • Servicing
ISO 13485 training focuses on a risk based approach to an organization's management system which demonstrates its ability to consistently provide products and services which meet customer and applicable statutory and regulatory requirements.
To enquire about ISO 13485 courses please complete the course enquiry form This form can also be used to enquire about holding any of these courses at your premises.
For other enquiries about training, please contact us by telephone on +44 7024077868 or email us at info@royalint.co.uk