In order to be able to continuously assess the criteria mentioned in I of Article L. 5121-12, the Haute Autorité de santé and, where applicable, the Agence nationale de sécurité du médicament et des produits de santé may at any time ask the holder of the exploitation rights for the medicinal product covered by the early access authorisation or, where applicable, its authorised representative, to send it data enabling it to assess whether these criteria continue to be met.