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Notification Detail :: G/TBT/N/GBR/4
Main Data
Notification No.
Notification Type
Notifying Member
Date of Notification
Final Date for Comments
Days to Final Date
Title
Draft Regulations, The Unlicensed ;Medicinal Products for Human Use (Transmissible Spongiform Encephalopathies) (Safety) Regulations S.I. 2002 Number of pages: 11 Language: English
Objective
Product Covered
Any medicinal products for human use which are supplied under UK law other than in accordance with a marketing authorization under either Directive 2001/83/EC or the UK national scheme for regulating medicines not covered by the Community scheme, the Medicines Act 1968. The two main categories of unlicensed medicines are: (a) medicines (commonly know as "specials") which are exempt from licensing because they are supplied in response to the unsolicited order of a doctor or dentist to meet the special needs of an individual patient on his direct personal responsibility; (b) medicines (excluding herbal remedies) mixed, assembled and supplied by someone who is not a doctor or dentist, (known as a "non-orthodoyx practitioner"), to a patient who has consulted him about his health. In addition, any substance which, although not requiring a marketing authorization is classified as a "medicinal product" with the united Kingdom, as is regulated accordingly
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FR:
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ES:
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