Real Decreto sobre Medicamentos Veterinarios (Real Decreto 109/1995, de 27 de Enero)

This document cites

• REAL DECRETO 1470/2001, de 27 de diciembre, </strong>por el que<strong> se modifica el Real Decreto 109/1995, de 27 de enero, sobre medicamentos veterinarios.
• Ley de régimen jurídico de las Administraciones Públicas y del Procedimiento Administrativo Común (Ley 30/1992, de 26 de noviembre) - Article 38
• Real Decreto de estructura Orgánica y Funciones del Instituto Nacional de la Seguridad Social y de modificación parcial de la Tesorería General de la Seguridad Social (Real Decreto 2583/1996, de 13 de diciembre)
• Constitución Española de 1978 - Article 149
• Ley General de Sanidad (Ley 14/1986, de 25 de abril) - Articles 6, 40



See all quotations

• Ley de Tasas y Precios Públicos (Ley 8/1989, de 13 de Abril)
• Ley del Medicamento (Ley 25/1990, de 20 de diciembre) - Articles 4, 43, 44, 45, 46, 47, 48, 49, 50, 55, 79, 83, 100, 105, 114, 116, 117, 118, 119
• Ley de Firma Electrónica (Ley 59/2003, de 19 de diciembre)
• Estatuto de la Agencia Española del Medicamento (Real Decreto 520/1999, de 26 de marzo)
• Ley de Garantías y Uso Racional de los Medicamentos y Productos Sanitarios (Ley 29/2006, de 26 de julio) - Articles 2, 3, 37
• LEY 42/1994, de 30 de Diciembre, de Medidas fiscales, administrativas y de Orden social.
• Real Decreto 418/1987, de 20 de Febrero, sobre las sustancias y Productos que intervienen en la alimentacion de los animales.
• REAL DECRETO 479/2004, de 26 de marzo, </strong>por el que<strong> se establece y regula el Registro general de explotaciones ganaderas. - Article 5
• REAL DECRETO 2178/2004, de 12 de noviembre, </strong>por el que<strong> se prohíbe utilizar determinadas sustancias de efecto hormonal y tireostático y sustancias beta-agonistas de uso en la cría de ganado.
• Real Decreto 1246/2008, de 18 de julio, </strong>por el que<strong> se regula el procedimiento de autori­zación, registro y farmacovigilancia de los medicamentos veterinarios fabricados industrialmente.
• Ley de Sanidad Animal (Ley 8/2003, de 24 de abril)
• Real Decreto por el que se desarrolla, en materia de Incapacidades laborales del Sistema de la Seguridad social, la Ley 42/1994, de 30 de Diciembre, de Medidas fiscales, administrativas y de Orden social (Real Decreto 1300/1995, de 21 de Julio)
• Real Decreto por el que se regulan los Laboratorios Farmacéuticos, los Fabricantes de Principios Activos de Uso Farmacéutico y el Comercio Exterior de Medicamentos y Medicamentos en Investigación (Real Decreto 824/2010, de 25 de junio)
• Real Decreto 1132/2010, de 10 de septiembre, </strong>por el que<strong> se modifica el Real Decreto 109/1995, de 27 de enero, sobre medicamentos veterinarios.
• Real Decreto 163/1981, de 23 de enero, sobre productos zoosanitarios y otras sustancias utilizadas en la producción animal.
• Real Decreto 504/2011, de 8 de abril, de estructura orgánica y funciones del Instituto Social de la Marina.
• Council Directive 90/677/EEC of 13 December 1990 extending the scope of Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products and laying down additional provisions for immunological veterinary medicinal products
• Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance )
• Commission Regulation (EC) No 1950/2006 of 13 December 2006 establishing, in accordance with Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products, a list of substances essential for the treatment of equidae and of substances bringing added clinical benefit (Text with EEA relevance)
• Commission Directive 92/18/EEC of 20 March 1992 modifying the Annex to Council Directive 81/852/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the texting of veterinary medicinal products
• Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
• 2000/68/EC: Commission Decision of 22 December 1999 amending Commission Decision 93/623/EEC and establishing the identification of equidae for breeding and production (notified under document number C(1999) 5004) (Text with EEA relevance)
• 93/623/EEC: Commission Decision of 20 October 1993 establishing the identification document (passport) accompanying registered equidae
• Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products
• Commission Directive 91/412/EEC of 23 July 1991 laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products
• Council Directive 87/22/EEC of 22 December 1986 on the approximation of national measures relating to the placing on the market of high-technology medicinal products, particularly those derived from biotechnology
• Council Directive 90/676/EEC Of 13 December 1990 amending Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products
• Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products
• Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (Text with EEA relevance)
• Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products