- Conduct the clinical investigation or other studies reported in scientific literature of a medical device for equivalence to the device.
- Review reports published in peer-reviewed scientific literature on other clinical experience of either the device.
- Maintain and update the PMCF/CER/CEP/LSP/LSR/PSUR documentation annually to justify the level of clinical evidence that conforms with the GSPR.
- Participate in overall post-market activities throughout the life cycle of the device.