Chwilio Deddfwriaeth

Chwiliad Uwch

The Medicines (Fees Relating to Medicinal Products for Human Use) Regulations 1989

Help about what version

Pa Fersiwn

  • Y Diweddaraf sydd Ar Gael (Diwygiedig)
  • Gwreiddiol (a wnaed Fel)

Status:

Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol). This item of legislation is currently only available in its original format.

  1. Introductory Text

  2. PART I GENERAL

    1. 1.Citation, commencement and scope

    2. 2.Interpretation

  3. PART II FEES FOR APPLICATIONS FOR LICENCES OR CERTIFICATES AND FOR INSPECTIONS IN CONNECTION THEREWITH

    1. 3.Applications for Licences

    2. 4.Applications for Clinical Trial Certificates

    3. 5.Applications for certificates for exports of medicinal products

  4. PART III FEES FOR APPLICATIONS FOR VARIATIONS OF LICENCES OR CERTIFICATES

    1. 6.Variations of Licences

    2. 7.Variations of Clinical Trial Certificates

    3. 8.Change of Name or Address in Clinical Trial Certificates

    4. 9.Applications for Multiple Variations

  5. PART IV FEES FOR APPLICATIONS FOR RENEWALS OF LICENCES OR CERTIFICATES

    1. 10.Renewal of Licences

    2. 11.Renewal of Certificates

    3. 12.Renewals in terms which are not identical to the existing licence or certificate

  6. PART V FEES FOR INSPECTIONS MADE DURING THE CURRENCY OF A LICENCE

    1. 13.(1) Subject to paragraph (4) below and to regulations 16...

  7. PART VI ADMINISTRATION

    1. 14.Payment of fees to Ministers

    2. 15.Time for payment of fees in connection with applications or inspections and refunds of such fees

    3. 16.Waiver, Reduction or Refund of Fees

    4. 17.Suspension of Licences

    5. 18.Civil proceedings to recover unpaid fees

  8. PART VII REVOCATION, SAVINGS AND TRANSITIONAL PROVISIONS

    1. 19.Revocation and Savings

    2. 20.Transitional provisions

  9. Signature

    1. SCHEDULE 1

      FEES FOR APPLICATIONS, VARIATIONS AND RENEWALS OF LICENCES

      1. PART I INTERPRETATION

        1. 1.In this Schedule — “active ingredient” means the ingredient of...

      2. PART II FEES FOR APPLICATIONS FOR LICENCES

        1. 1.Product Licences

        2. 2.Where a major application is made by a person who...

        3. 3.(1) Subject to sub-paragraphs (2) and (3) below, where an...

        4. 4.Manufacturers' Licences

        5. 5.Wholesale Dealers' Licences

      3. PART III FEES FOR APPLICATIONS FOR VARIATIONS OF LICENCES

        1. 1.Product Licences

        2. 2.Manufacturers' Licences

        3. 3.Wholesale Dealers' Licences

        4. 4.Other Variations

      4. PART IV FEES FOR APPLICATIONS FOR RENEWALS OF LICENCES

        1. 1.Product Licences

        2. 2.Manufacturers' Licences

        3. 3.Wholesale Dealers' Licences

    2. SCHEDULE 2

      FEES FOR INSPECTIONS

      1. 1.Interpretation

      2. 2.Fees

      3. 3.(1) Subject to sub-paragraph (2) below, unless the applicant or,...

      4. 4.In the case of an inspection in connection with the...

      5. 5.The fee payable in respect of an inspection at a...

    3. SCHEDULE 3

      WAIVER, REDUCTION OR REFUND OF FEES

      1. 1.Where the manufacture, assembly, sale or supply of medicinal products...

      2. 2.(1) Subject to sub-paragraph (2) below, where an application for...

      3. 3.Where an application for a manufacturer’s or a wholesale dealer’s...

      4. 4.Where the same site is inspected at the same time...

    4. SCHEDULE 4

      REGULATIONS REVOKED IN SO FAR AS THEY APPLY IN RELATION WHOLLY OR PARTLY TO MEDICINAL PRODUCTS FOR HUMAN USE

      1. The Medicines (Fees) Regulations 1978 The Medicines (Fees) Amendment Regulations...

  11. Explanatory Note

Yn ôl i’r brig

Options/Help

Print Options

Close

Mae deddfwriaeth ar gael mewn fersiynau gwahanol:

Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.

Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.

Close

Dewisiadau Agor

Dewisiadau gwahanol i agor deddfwriaeth er mwyn gweld rhagor o gynnwys ar y sgrin ar yr un pryd

Close

Rhagor o Adnoddau

Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:

  • y PDF print gwreiddiol y fel deddfwyd fersiwn a ddefnyddiwyd am y copi print
  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • slipiau cywiro
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill
Close

Rhagor o Adnoddau

Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:

  • y PDF print gwreiddiol y fel gwnaed fersiwn a ddefnyddiwyd am y copi print
  • slipiau cywiro

liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys

  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill