Draft amendments to the Rules for marketing authorization and assessment of medicinal products for human use; (24 page(s), in Russian)

Draft Amendments to Article 7 and to the Annex to Article 4 of the "Regulations Governing the Classification of Medical Devices"; (43 page(s), in English), (27 page(s), in Chinese)

Medical Devices Subject to Administrative Destruction; (9 page(s), in English)