Medicines legislation and regulation in the United Kingdom 1500-2020

11Citations
Citations of this article
41Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The initial purposes of regulation of medicines in England, and latterly in the United Kingdom, were principally to raise government revenue, to discourage murder by poisoning and to regulate the activities of pharmacists. It was only much later that regulators sought to ensure that medicines were of good quality, reasonably safe, and at least somewhat effective, and to curtail misuse of drugs. Here we survey the history of the regulation of medicines and poisons in England from the perspective of clinicians with an interest in therapeutics.

Cite

CITATION STYLE

APA

Ferner, R. E., & Aronson, J. K. (2023, January 1). Medicines legislation and regulation in the United Kingdom 1500-2020. British Journal of Clinical Pharmacology. John Wiley and Sons Inc. https://doi.org/10.1111/bcp.15497

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free