- Latest available (Revised)
- Original (As made)
This is the original version (as it was originally made).
6.Meaning of “unbranded generic health service medicine” and listing of a presentation of unbranded generic health service medicine
7.Information to be recorded and kept about supply of unbranded generic health service medicines: manufacturers and importers
8.Information to be recorded and kept about supply of unbranded generic health service medicines: medicines wholesalers
9.Requirement to provide information about supply of unbranded generic health service medicines
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
11.Information to be recorded about supply of made special health service medicines: manufacturers
12.Information to be recorded about supply of made special health service medicines: medicines wholesalers
13.Information to be recorded and kept about supply of imported special health service medicines: medicines wholesalers and importers
14.Requirement to provide information about the supply of special health service medicines
16.Information to be recorded and kept about supply of imported special health service medicines: medicines wholesalers and importers
17.Information to be recorded and kept about supply of health service medicines other than imported special health service medicines: medicines wholesalers
18.Information to be recorded and kept about supply of health service medicines other than imported special health service medicines: other UK producers
19.Information to be recorded and kept about supply of health service medicines to patients otherwise than by sale
20.Information to be recorded and kept about supply of health service appliances: manufacturers and importers
21.Information to be recorded and kept about supply of listed health service appliances: medical supplies wholesalers
22.Information to be recorded and kept about supply of appliances, food and dermatological products to patients otherwise than by sale
23.Provision of information recorded and kept under this Part to the Secretary of State
25.Provision of information about costs incurred in connection with the manufacture or distribution of a particular health service medicine or appliance
26.Provision of general information about costs incurred in connection with the manufacture or distribution of health service medicines and appliances
27.Provision of information about English health service medicines which are not available at the reimbursement price
28.Provision of information about availability of health service medicines
29.Requirement to provide information about discontinuation or anticipated supply shortage of certain health service medicines
2.Transitional provision: information about supply of unbranded generic health service medicines
3.Circumstances in which transitional provision in paragraph 2 ceases to apply
4.Transitional provision: information about supply of special health service medicines
5.Circumstances in which transitional provision in paragraph 4 ceases to apply
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Instrument and provides information about its policy objective and policy implications. They aim to make the Statutory Instrument accessible to readers who are not legally qualified and accompany any Statutory Instrument or Draft Statutory Instrument laid before Parliament from June 2004 onwards.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
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:
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including: