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The Human Medicines Regulations 2012

Schedule 8 Material to accompany an application for a UK marketing authorisation

United Kingdom

1General requirements
2Summary of the product characteristics

← Paragraph 24

Schedule 8

Paragraph 1 →

Legislation: The Human Medicines Regulations 2012
Citation: S.I. 2012/1916, schedule 8
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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