When a medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area carries out the analytical phase of medical biology examinations begun in France, the accreditation conditions, the authorisation conditions or the approval conditions referred to in 1° and 2° of Article L. 6221-4 are recognised as equivalent to those laid down for medical biology laboratories established on French territory, provided that these conditions comply with the criteria defined by the harmonised standards applicable to medical biology laboratories, the references of which are set by the interministerial order referred to in I of Article L. 6221-2.