The application for an import authorisation must be sent by any means capable of providing a date certain and must indicate :
1° The name or business name and address of the natural or legal person responsible for the import or, for gene therapy or xenogenic cell therapy preparations, the name and address of the establishment or body authorised under Article L. 4211-8 or Article L. 4211-9;
2° The country of origin and, if different, the country of origin of the medicinal product;
3° Its name, composition, pharmaceutical form, strength and route of administration;
4° The quantities imported;
5° The purpose of the import.