Show Summary Details
Medical LawText, Cases, and Materials

Medical Law: Text, Cases, and Materials (5th edn)

Emily Jackson
Page of

Printed from Oxford Law Trove. Under the terms of the licence agreement, an individual user may print out a single article for personal use (for details see Privacy Policy and Legal Notice).

date: 21 March 2023

p. 57311. The Regulation of Medicineslocked

p. 57311. The Regulation of Medicineslocked

  • Emily JacksonEmily JacksonProfessor of Law, London School of Economics


All books in this flagship series contain carefully selected substantial extracts from key cases, legislation, and academic debate; providing students with a stand-alone resource. This chapter examines the regulation of medicines. It first explains what a medicine is and the need for it to have a marketing authorization before it can be put into circulation. It covers the importance not only of establishing safety and efficacy before licensing, but afterwards as well, through pharmacovigilance mechanisms. The chapter covers the increasing European harmonization of the rules covering the licensing and marketing of medicines, and briefly discusses the implications of Brexit. Finally, it looks at liability for defective medicines, and the strict liability regime under the Consumer Protection Act.

You do not currently have access to this chapter

Sign in

Please sign in to access the full content.


Access to the full content requires a subscription