SIFo Medical has access to a network of industry experts with years of experience in Quality Management, whom our clients can consult to ensure they meet industry regulatory standards such as the European Union’s MDR 2017/745. Our services cover process validation, test method validation, product development, design control, packaging validation and risk management.

In addition to flawless, up-to-date technical documentation, our experts can improve your processes and bring them to peak performance in the shortest possible time.

  • Use a proven structured system to build a compliant Quality Management System (QMS) to produce safe medical devices.
  • Benefit from our experts’ knowledge and experience to make your QMS audit-proof & gain maximum security.
  • Save time and costs in the long-run by using our best practices to establish efficient production processes, compliant documentation, reduce complaint rates and source qualitative parts and components at competitive prices
  • Receive hands-on support, timely results and individual focus on your issues.
  • Profit from maximum knowledge transfer and count on an exclusive network of quality experts and suppliers supporting and actively assisting you in all matters of quality management

For more information on our QM consulting services, contact us via the enquiry form on our profile (linked above).