ISO 14971 Risk management for medical devices

Optimize your risk management system

ISO 14971 risk management medical devicesIn the medical device industry, risk management goes beyond development and manufacturing; it is a vital part of all your company’s processes. ISO 14971 defines the international requirements of risk management systems for medical devices, defining best practices throughout the entire life cycle of a device.

To ensure your company gets a safe, effective product to market on time and within budget, you need a successful implementation of your risk management system.

What are the benefits of ISO 14971?

  • Implement ideal methods of reducing risk for all stakeholders
  • Develop devices and therapies that are proven effective in the industry
  • Manage speed and cost to market
  • Optimize speed of iteration
  • Streamline the regulatory process that will enable entry to selected markets