Authorised bodies 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° How the samples are prepared;
4° The origin of the samples and how they were obtained;
5° Depending on the cases provided for in Article L. 1211-2, details of consent or absence of opposition;
6° The contact details of the transferees and details of their research activity;
7° The place of storage.
The Minister responsible for research and, where applicable, the Director General of the Regional Health Agency may also request information from the organisation at any time to enable them to ensure that the activities are being carried out in compliance with the legislative and regulatory provisions and the requirements mentioned in the second paragraph of Article R. 1243-62.