Governmental Decree No.686 of 6 July 2012 validating the Regulation on licensing the production of medicines. País/Territorio Federación de Russia Tipo de documento Reglamento Fecha 2012 (2019) Fuente FAO, FAOLEX Materia Ganado Palabra clave Sanidad animal Medicamentos Negocios/industria/corporaciones Autorización/permiso Área geográphica Ártico, Asia y Pacifico, Mar Negro, Mar Caspio, CEI (Comunidad de Estados Independientes), Europa Oriental, Europa, Europa y Central Asia, Pacífico Norte, Pacífico Nordoeste Resumen This Governmental Decree provides requirements for pharmaceutical manufactures in order to obtain a license for medicines production. The Federal Veterinary and Phytosanitary Supervision Service issues licenses for VMP production. Licensing requirements for applicant shall be as follows: (a) of premises and equipment required for the performance of pharmaceutical activities; (b) compliance with good practices requirements and quality control of production; (c) availability of technical regulations, including data related to used pharmaceutical substances and additives; (d) availability of the head of organization 5-year higher pharmaceutical, chemical, medical or biological education and 5-year working experience; and (e) availability of medical staff on contractual basis. Annex I contains the list of pharmaceutical activities subject to mandatory licensing. Texto completo Ruso Página web pravo.gov.ru