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The Human Medicines Regulations 2012
Schedule 12
Part 1

Paragraph 5

A description of the methods of manufacturing the medicinal product.

← Paragraph 4

Paragraph 5

Paragraph 6 →

Legislation: The Human Medicines Regulations 2012
Citation: S.I. 2012/1916, paragraph 5
Versions: Latest · As made
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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