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The Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994
Schedule 1

Paragraph 6

Changes not yet applied. Later legislation changes this provision in ways not yet written into the text below:

Sch 1 rev by Medicines (Homoeopathic Medicinal Products for Human Use) 2005 reg 16

A copy of the manufacturer’s licence or corresponding authorisation granted by a member State other than the United Kingdom in respect of the product.

← Paragraph 5

Paragraph 6

Paragraph 7 →

Legislation: The Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994
Citation: S.I. 1994/105, paragraph 6
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright
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