# Human Fertilisation and Embryology Act 1990, Paragraph 3


In relation to Great Britain, licence conditions shall require such—
(a) systems to report, investigate, register and transmit information about serious adverse events and serious adverse reactions, and
(b) accurate, rapid and verifiable procedures for recalling from distribution any product which may be related to a serious adverse event or serious adverse reaction,
to be in place as the Authority considers appropriate.

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Source: https://www.legislation.gov.uk/ukpga/1990/37/schedule/3A/paragraph/3 (the official version)
Page: https://openlegislation.uk/human-fertilisation-and-embryology-act-1990/schedule-3A/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.