The Medicines for Human Use (Fees and Miscellaneous Amendments) Regulations 2003

This document cites

• European Communities Act 1972
• Finance Act 1973
• Medicines Act 1971
• Health and Medicines Act 1988
• Medicines Act 1968



See all quotations

• Northern Ireland Act 2000
• Northern Ireland Act 1998
• Departments (Northern Ireland) Order 1999
• Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994
• Medicines (Products for Human Use-Fees) Amendment Regulations 1996
• Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 2002
• Medicines (Applications for Grant of Product Licences-Products for Human Use) Regulations 1993
• Transfer of Functions (Medicines and Poisons) Order 1999
• Transfer of Functions (Wales) Order 1969
• European Communities (Designation) Order 1972
• Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994
• Medicines for Human Use (Marketing Authorisation Etc.) Amendment Regulations 1998
• Medicines (Advertising) Regulations 1994
• Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 1998
• Medicines (Codification Amendments Etc.) Regulations 2002
• Medicines (Products for Human Use - Fees) Regulations 1995
• Ministry of Agriculture, Fisheries and Food (Dissolution) Order 2002
• Medicines (Standard Provisions for Licences and Certificates) Regulations 1971
• Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use