Chwilio Deddfwriaeth

Chwiliad Uwch

The Human Medicines Regulations 2012

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Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol).

PART 3Small immediate packaging

18.  The scientific name of the stock or stocks (which may be supplemented by an invented name if the product contains two or more stocks), and the degree of dilution, making use of the symbols of the European Pharmacopoeia or, in the absence of an entry in the European Pharmacopoeia, of the British Pharmacopoeia.

19.  The name and address of the holder of the certificate of registration.

20.  The method and, if necessary, route of administration.

21.  The product’s expiry date (month and year), in clear terms.

22.  The contents of the presentation, specified by weight, volume or number of doses.

23.  The manufacturer’s batch number.

24.  The words “homoeopathic medicinal product without therapeutic indications”.

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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:

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