Within ninety days of the end of the research involving human subjects, the sponsor must inform the competent authority and the relevant data protection committee of the effective date of the end of the research, corresponding to the end of the participation of the last person to take part in the research or, where applicable, the end date defined in the protocol.
If the termination of the research involving the human person is anticipated, the sponsor must provide this information within a period of fifteen days and communicate the reasons.
The content and methods of presentation of the information relating to the end of the research are laid down, where necessary, by order of the Minister for Health, made on a proposal from the Director General of the National Agency for the Safety of Medicines and Health Products for research falling within its remit.