When the National Agency for the Safety of Medicines and Health Products, the High Authority for Health, the Minister for Health or the European Medicines Agency refers a non-interventional research project involving a medicinal product which has been granted a marketing authorisation to the Committee for the Protection of Individuals for an opinion, it shall give the opinion referred to in Article L. 1123-7 solely with regard to the requirements mentioned in the third paragraph of Article L. 1124-1.