Health establishments, organisations, health cooperation groupings and medical biology laboratories authorised to carry out medically assisted procreation activities are subject to inspection or control by the agents mentioned in article L. 1421-1, at least every two years.
Under the authority of the Minister for Health, the Director General of the Regional Health Agency shall communicate to the competent authorities of the other Member States of the European Union or parties to the Agreement on the European Economic Area and to the European Commission all information on the results of inspections and other control measures relating to establishments which import gametes and germ tissue.