The Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005

This document cites

• European Communities Act 1972
• Medicines Act 1971
• Health and Social Care Act 2001
• Medicines Act 1968
• Northern Ireland Act 2000



See all quotations

• Northern Ireland Act 1998
• Departments (Northern Ireland) Order 1999
• Medicines (Veterinary Drugs) (Renewal Applications for Licences and Animal Test Certificates) Regulations 1993
• Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994
• The Medicines (Traditional Herbal Medicinal Products for Human Use) Regulations 2005
• Medicines (Retail Sale or Supply of Herbal Remedies) Order 1977
• Medicines (Applications for Manufacturer's and Wholesale Dealer's Licences) Regulations 1971
• Transfer of Functions (Medicines and Poisons) Order 1999
• Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1994
• Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994
• Medicines Act 1968 (Amendment) Regulations 1993
• The Medicines for Human Use (Clinical Trials) Regulations 2004
• Medicines (Medicines Act 1968 Amendment) Regulations 1977
• Ministry of Agriculture, Fisheries and Food (Dissolution) Order 2002
• Medicines (Applications for Manufacturer's and Wholesale Dealer's Licences) Amendment Regulations 1977
• Medicines (Renewal Applications for Licences and Certificates) Regulations 1974
• Medicines (Standard Provisions for Licences and Certificates) Regulations 1971
• Commission Directive 2003/94/EC of 8 October 2003 laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use (Text with EEA relevance)