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The Medicated Feedingstuffs Regulations 1998

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  1. Introductory Text

  2. PART I GENERAL

    1. 1.Title and commencement

    2. 2.Interpretation

  3. PART II APPROVAL OF PREMISES

    1. 3.Applications for the approval of premises

    2. 4.Approval of premises

    3. 5.Renewal of approvals

    4. 6.Late renewal

    5. 7.Grant of renewal

    6. 8.Withdrawal of approvals

    7. 9.Procedure relating to the withdrawal of approvals

  4. PART III APPROVAL OF DISTRIBUTORS

    1. 10.Applications for the approval of distributors

    2. 11.Approval of distributors

    3. 12.Renewal of approvals

    4. 13.Late renewal

    5. 14.Grant of renewal

    6. 15.Withdrawal of approvals

    7. 16.Procedure relating to the withdrawal of approvals

  5. PART IV CONTROL OF AGRICULTURAL MERCHANTS

    1. 17.Prohibition notice on agricultural merchant

  6. PART V CONTROL OF AUTHORISED MEDICATED PRE-MIXES

    1. 18.Retail supply of authorised medicated pre-mixes

    2. 19.Duties on persons engaged in the retail supply of authorised medicated pre-mixes

  7. PART VI CONTROL OF INTERMEDIATE PRODUCTS

    1. 20.Manufacture of intermediate products

    2. 21.Retail supply of authorised intermediate products

    3. 22.Duties on persons engaged in the retail supply of authorised intermediate products

    4. 23.Labelling and packaging of intermediate products

  8. PART VII CONTROL OF MEDICATED FEEDINGSTUFFS

    1. 24.Manufacture of medicated feedingstuffs

    2. 25.Packaging of medicated feedingstuffs

    3. 26.Labelling of medicated feedingstuffs

    4. 27.Restrictions on the holding, placing on the market and use of medicated feedingstuffs

    5. 28.Supply of medicated feedingstuffs

    6. 29.MFS prescriptions

    7. 30.Restrictions on the quantity of medicated feedingstuffs that may be supplied

    8. 31.Restrictions on the slaughter of treated animals and the disposal of products obtained from such animals

    9. 32.Import of medicated feedingstuffs from E.E.A. States

    10. 33.Import of medicated feedingstuffs from third countries

    11. 34.Export of medicated feedingstuffs to E.E.A. States

  9. PART VIII MISCELLANEOUS AND SUPPLEMENTAL PROVISIONS

    1. 35.Recovery of fees

    2. 36.Sampling checks and enforcement

    3. 37.Powers of authorised persons

    4. 38.Offences

    5. 39.Punishment of offences

    6. 40.Offences by bodies corporate and Scottish partnerships

    7. 41.Defence

    8. 42.Service of notices

    9. 43.Exclusion of the application of the Medicines Act 1968

  10. Signature

  11. THE SCHEDULES

    1. Schedule 1

      Fees

    2. Schedule 2

      Interpretation:

      1. Part I Expressions having the same meaning as in the Medicated Feedingstuffs Directive.

      2. Part II Expressions having the same meaning as in Directive 81/851/EEC.

    3. Schedule 3

      Approval of Premises: Matters to be taken into account.

    4. Schedule 4

      Approval of Distributors: Matters to be taken into account.

  12. Explanatory Note

Yn ôl i’r brig

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