When a medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area which is not on the list referred to in Article D. 6221-6 carries out the analytical phase of a medical biology examination begun in France, the authorisation provided for in 3° of Article L. 6221-4 is granted provided that its operating conditions comply with the criteria defined by the harmonised standards whose references are set by the interministerial order provided for in I of Article L. 6221-2 and that the procedures for verification by a third-party body of compliance with these criteria are equivalent to those provided for in the accreditation procedure applicable in France.