# The Human Medicines Regulations 2012, Regulation 185: Recording obligations on the licensing authority


The licensing authority must record all suspected adverse reactions to medicinal products that—
(a) occur in the United Kingdom; and
(b) are reported to it by a holder, a patient or a patient's carer, a health care professional, a coroner or a procurator fiscal.

---
Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/185 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-185
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.