Chwilio Deddfwriaeth

The Health Service Products (Provision and Disclosure of Information) Regulations 2018

Changes to legislation:

There are currently no known outstanding effects for the The Health Service Products (Provision and Disclosure of Information) Regulations 2018. Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

  1. Introductory Text

  2. PART 1 Introductory

    1. 1.Citation and commencement

    2. 2.Interpretation: general

    3. 3.Application

    4. 4.Exception: products not known to be health service products

    5. 5.Information required to be provided via an NHS England online gateway

  3. PART 2 Quarterly information about unbranded generic health service medicines

    1. 6.Meaning of “unbranded generic health service medicine” and listing of a presentation of unbranded generic health service medicine

    2. 7.Information to be recorded and kept about supply of unbranded generic health service medicines: manufacturers and importers

    3. 8.Information to be recorded and kept about supply of unbranded generic health service medicines: medicines wholesalers

    4. 9.Requirement to provide information about supply of unbranded generic health service medicines

  4. PART 3 Quarterly information about special health service medicines

    1. 10.Meaning of “special health service medicine”, “imported special health service medicine”, “made special health service medicine” and listing of a presentation of special health service medicine in a Drug Tariff

    2. 11.Information to be recorded about supply of made special health service medicines: manufacturers

    3. 12.Information to be recorded about supply of made special health service medicines: medicines wholesalers

    4. 13.Information to be recorded and kept about supply of imported special health service medicines: medicines wholesalers and importers

    5. 14.Requirement to provide information about the supply of special health service medicines

  5. PART 4 General information about supply of UK health service products

    1. 15.Categories of purchaser

    2. 16.Information to be recorded and kept about supply of imported special health service medicines: medicines wholesalers and importers

    3. 17.Information to be recorded and kept about supply of health service medicines other than imported special health service medicines: medicines wholesalers

    4. 18.Information to be recorded and kept about supply of health service medicines other than imported special health service medicines: other UK producers

    5. 19.Information to be recorded and kept about supply of health service medicines to patients otherwise than by sale

    6. 20.Information to be recorded and kept about supply of health service appliances: manufacturers and importers

    7. 21.Information to be recorded and kept about supply of listed health service appliances: medical supplies wholesalers

    8. 22.Information to be recorded and kept about supply of appliances, food and dermatological products to patients otherwise than by sale

    9. 23.Provision of information recorded and kept under this Part to the Secretary of State

    10. 24.Provision of information: small producers

  6. PART 5 Information about costs incurred in connection with the manufacturing, distribution or supply of UK health service products

    1. 25.Provision of information about costs incurred in connection with the manufacture or distribution of a particular health service medicine or appliance

    2. 26.Provision of general information about costs incurred in connection with the manufacture or distribution of health service medicines and appliances

  7. PART 6 Information about price and availability of health service medicines

    1. 27.Provision of information about English health service medicines which are not available at the reimbursement price

    2. 28.Provision of information about availability of health service medicines

    3. 29.Requirement to provide information about discontinuation or anticipated supply shortage of certain health service medicines

  8. PART 7 Information about reasonable estimates

    1. 30.Requirement to provide information about reasonable estimates

  9. PART 8 Enforcement and appeals

    1. 31.Compliance procedure

    2. 32.Penalties

    3. 33.Appeals

  10. PART 9 Disclosure of information

    1. 34.Disclosure of information

  11. PART 10 Miscellaneous

    1. 35.Transitional provisions

    2. 36.Annual review

  12. Signature

    1. SCHEDULE 1

      Interpretation: general

      1. 1.Interpretation: general

      2. 2.Meaning of “presentation of health service medicine”

      3. 3.Meaning of “UK primary medical services provider”, “Health Service chemist” and related expressions

      4. 4.Meaning of “net NHS expenditure”, “net NHS wholesale income”, “net purchase amount” and “net sales income”

      5. 5.Meaning of “NHS framework contract”

      6. 6.Interpretation: listing of an appliance in a Drug Tariff

    2. SCHEDULE 2

      Small producers

      1. 1.General

      2. 2.Interpretation of Schedule 2

      3. 3.UK primary medical providers who are small producers

      4. 4.Health Service chemists who are small producers

      5. 5.NHS hospital purchasers who are small producers

      6. 6.Other UK producers who are small producers

    3. SCHEDULE 3

      Calculation of daily penalty

      1. 1.Interpretation of Schedule 3

      2. 2.Daily penalty payable by UK producers who are small producers

      3. 3.Daily penalty payable by UK producers who are not small producers

    4. SCHEDULE 4

      Disclosure of information under section 246B of the 2006 Act: prescribed bodies and prescribed purposes

      1. 1.(1) The bodies specified in column 1 of Table 1,...

      2. 2.(1) The bodies specified in column 1 of Table 2...

    5. SCHEDULE 5

      Information about supply of unbranded generic health service medicines or special health service medicines: transitional provisions

      1. 1.General

      2. 2.Transitional provision: information about supply of unbranded generic health service medicines

      3. 3.Circumstances in which transitional provision in paragraph 2 ceases to apply

      4. 4.Transitional provision: information about supply of special health service medicines

      5. 5.Circumstances in which transitional provision in paragraph 4 ceases to apply

  13. 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

Memorandwm Esboniadol

Mae Memoranda Esboniadol yn nodi datganiad byr o ddiben Offeryn Statudol ac yn rhoi gwybodaeth am ei amcan polisi a goblygiadau polisi. Maent yn ceisio gwneud yr Offeryn Statudol yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol, ac maent yn cyd-fynd ag unrhyw Offeryn Statudol neu Offeryn Statudol Drafft a gyflwynwyd ger bron y Senedd o Fehefin 2004 ymlaen.

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

Asesiadau Effaith

Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:

  • Why the government is proposing to intervene;
  • The main options the government is considering, and which one is preferred;
  • How and to what extent new policies may impact on them; and,
  • The estimated costs and benefits of proposed measures.
Close

Llinell Amser Newidiadau

This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.

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