Human Medicines Regulations 2012

Short description: United Kingdom legislation

Human Medicines Regulations 2012Statutory Instrument

Citation| 2012 No. 1916
Territorial extent| United Kingdom
Dates
Made| 19 July 2012
Laid before Parliament| 24 July 2012
Commencement| 14 August 2012 (2012-08-14)
Repealed|  ()
Other legislation
Amends| Medicines Act 1968
Transposes| Directive 2010/84/EU
Amended by| The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020

Status: Current legislation

Text of statute as originally enacted

The Human Medicines Regulations 2012 in the United Kingdom were created, under statutory authority of the European Communities Act 1972 and the Medicines Act 1968 in 2012. The body responsible for their upkeep is the Medicines and Healthcare products Regulatory Agency. The regulations partially repealed the Medicines Act 1968 in line with EU legislation.[1][2][3][4]

## Contents

* 1 Amendments
* 2 Regulation 174
* 3 References
* 4 External links

## Amendments

In October 2020, the regulations were amended to expand the workforce eligible to administer COVID-19 vaccines, so enabling additional healthcare professionals to vaccinate the public. This was a temporary provision, but in January 2022 it was announced that this would be made permanent as would the provision for community pharmacy contractors to provide COVID-19 and flu vaccines “away from their normal registered premises”.[5]

## Regulation 174

Regulation 174 provides an exemption to the requirement for authorisation of Regulation 46, allowing for the sale or supply of any medicinal product to be temporarily authorised by the licensing authority (MHRA) in response to the suspected or confirmed spread of pathogenic agents, toxins, chemical agents or nuclear radiation.[6]

## References

1. ↑ "How will the new Human Medicines Regulations affect your practice?". Royal Pharmaceutical Society. 3 August 2012. https://www.pharmaceutical-journal.com/news-and-analysis/how-will-the-new-human-medicines-regulations-affect-your-practice/11104804.article.
2. ↑ Medicines, Ethics and Practice 39: The professional guide for pharmacists. Royal Pharmaceutical Society of Great Britain. 18 July 2015. p. 25.
3. ↑ Appelbe, Gordon E.; Wingfield, Joy (2013). Dale and Appelbe's Pharmacy and Medicines Law (10 ed.). Pharmaceutical Press. p. 22. ISBN 9780853699897. https://books.google.com/books?id=wv47n8SvwsoC.
4. ↑ "Legislation covering medicines". Department of Health (N.I.). 18 August 2015. https://www.health-ni.gov.uk/articles/legislation-covering-medicines. "Please note that the Human Medicines Regulations 2012 repealed aspects of the Medicines Act 1968 as follows..."
5. ↑ "Law to be changed permanently to allow pharmacies to provide vaccinations off-premises". Pharmaceutical Journal. 26 January 2022. https://pharmaceutical-journal.com/article/news/government-to-enact-permanent-legislation-allowing-pharmacies-to-provide-vaccinations-off-premises.
6. ↑ Dodds-Smith, Ian; Townsend, Ewan (2017). "Unlicencsed Medicinal Products in the UK". Thompson Reuters Practical Law. https://www.arnoldporter.com/~/media/files/perspectives/publications/2017/02/unlicensed-medicinal-products-in-the-uk.pdf. "Regulation 174 contains an exemption for the sale or supply of products that are authorised by the MHRA on a temporary basis in response to the suspected or confirmed spread of pathogenic agents, toxins, chemical agents, or nuclear radiation, which may cause harm to human beings."

## External links

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