Any establishment or body which imports or exports organs for therapeutic purposes, including biomedical research within the meaning of Article L. 1121-1, shall ensure that these organs have been removed in compliance with standards of protection at least as stringent as the health safety rules mentioned in Article L. 1211-6 and standards of good practice at least equivalent to those provided for in Article L. 1235-5. He must be able to justify that he has ensured this.
The imported or exported organ must also be accompanied by the document mentioned in article R. 1211-19.