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The Excessive Regulation of Early Abortion Medication in the United Kingdom: The Case for Reform

Romanis, Elizabeth Chloe; Mullock, Alexandra; Parsons, Jordan A

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Authors

Alexandra Mullock

Jordan A Parsons



Abstract

Early medical abortion (EMA) involves the administration of two medications—mifepristone and misoprostol—24–48 hours apart. These routinely used medications are recognised as safe and effective by the World Health Organization which recommends this combination of medications as a safe form of abortion until nine weeks’ gestation. Despite the safety and effectiveness of this drug regimen, there exists excessive regulation around EMA. This is despite new regulations introduced in Northern Ireland in 2020 and (temporary) changes made in 2020 to allow at-home administration of mifepristone in Great Britain (following earlier changes to permit home use of misoprostol). We argue that the excessive regulation of EMA is inappropriate because it fails to recognise that abortion is essential healthcare. Further, the regulation constitutes disproportionate interference with clinical discretion and service organisation because it is medically unnecessary and prevents abortion providers in the UK from adapting their service provision in line with emerging evidence of best practice.

Citation

Romanis, E. C., Mullock, A., & Parsons, J. A. (2022). The Excessive Regulation of Early Abortion Medication in the United Kingdom: The Case for Reform. Medical Law Review, 30(1), 4-32. https://doi.org/10.1093/medlaw/fwab042

Journal Article Type Article
Acceptance Date Oct 21, 2021
Online Publication Date Dec 15, 2021
Publication Date 2022
Deposit Date Oct 25, 2021
Publicly Available Date May 25, 2022
Journal Medical Law Review
Print ISSN 0967-0742
Electronic ISSN 1464-3790
Publisher Oxford University Press
Peer Reviewed Peer Reviewed
Volume 30
Issue 1
Pages 4-32
DOI https://doi.org/10.1093/medlaw/fwab042

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