When, as part of its inspection powers, the Agence nationale de sécurité du médicament et des produits de santé finds that the manufacture or repackaging and relabelling for distribution of raw materials for pharmaceutical use complies with the good practices provided for in Article L. 5138-3, it issues a certificate of compliance, except for the distribution of excipients.
Any establishment carrying out one of the activities mentioned in the first paragraph may ask the Agency to certify that it complies with these good practices.
The model certificate of compliance shall be drawn up by the Agency in cooperation with the European Medicines Agency.