1. Patients have the right to access all information relevant to their implant, including known risks, adverse events, device limitations, software updates, and significant changes to the device.
  2. Health care professionals should provide patients with sufficient information to support informed consent throughout the life of the implant.
  3. Regulators should make safety findings, enforcement actions, and recall information easily available to the public.
  4. Where possible, aspects of the implant process including management, should remain under the management of health care professionals over the manufacturer and automated systems.