The investigator notifies the sponsor of adverse events and abnormal test results defined in the protocol as relevant to the evaluation of the safety of the donor, the person undergoing medically assisted reproduction or the child born or to be born, in accordance with the reporting requirements defined in the protocol and within the time limits specified therein.
In the notifications and in subsequent reports, the donor, the person who has undergone medically assisted procreation or the child born or to be born are identified by a code number.
The investigator provides the sponsor with additional information concerning serious adverse events. The sponsor must provide any additional information requested by the Data Protection Committee concerning reported cases of death.