Authorised bodies shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn or refused. They shall make any additional relevant information available to the Director General on request.
They inform the other organisations authorised in France or by any other Member State of the European Union or party to the Agreement on the European Economic Area and published in the Official Journal of the European Union of all certificates suspended, withdrawn or refused and, at their request, of certificates issued. They shall also make available to these bodies, at their request, any additional relevant information.