Medicines (Veterinary Medicinal Products) (Applications for Product Licences) Regulations 1993

This document cites

• European Communities Act 1972
• Northern Ireland Constitution Act 1973
• Northern Ireland Act 1974
• Medicines Act 1968
• Animals (Scientific Procedures) Act 1986



See all quotations

• Medicines (Labelling) Regulations 1976
• Medicines (Labelling of Medicinal Products for Incorporation in Animal Feeding Stuffs and of Medicated Animal Feeding Stuffs) Regulations 1988
• Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Amendment Regulations 1972
• Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Regulations 1971
• Transfer of Functions (Wales) (No. 1) Order 1978
• Transfer of Functions (Wales) Order 1969
• Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Amendment Regulations 1975
• Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Amendment Regulations 1983
• Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Amendment Regulations 1977
• Medicines (Labelling) Amendment Regulations 1977
• Medicines (Standard Provisions for Licences and Certificates) Regulations 1971
• 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
• 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
• 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
• Council Directive 81/852/EEC of 28 September 1981 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
• Council Directive 81/851/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to veterinary medicinal products
• The Medicines (Standard Provisions for Licences and Certificates) Amendment Regulations 1972