These Regulations amend the Medicated Feedingstuffs Regulations 1998 and continue to implement Council Directive 90/167/EEC laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community. They provide for new fees for applications for approval or renewal of: premises manufacturing authorized intermediate products; premises which manufacture medicated feedingstuffs incorporating medicated pre-mixes; and distributors of medicated feedingstuffs. The existing fee structure is changed and simplified. Previously, different fees were payable on an initial application for an approval, an application on renewal of an approval, and an application for an approval made outside the time limits in the Regulations. The new system specifies one fee for each of these applications. The previous fees are shown in the Schedule for comparison purposes.
United Kingdom of Great Britain and Northern Ireland · 2002-04-23