Within the scope of the declaration, organisations must be able to provide the following information at any time:
1° The nature and number of samples held;
2° The characteristics of the samples held;
3° The origin of the samples and how they were obtained;
4° The sample preparation procedures;
5° The research project;
6° Depending on the cases provided for in Article L. 1211-2, details of consent or lack of opposition;
7° The place of storage;
8° The destination of the samples at the end of the research project.
The Minister responsible for research or, where applicable, the Director General of the Regional Health Agency may also request information from the organisation at any time to ensure that the activities are being carried out in compliance with the legislative and regulatory provisions in force and meet the requirements set out in Article L. 1243-3.