Decision

June 2019: Promotion of PALEXIA® SR prolonged-release tablet by Grünenthal Ltd

Published 17 July 2019

The MHRA has a statutory duty to ensure that advertising of medicinal products within the UK conforms with Part 14 of the Human Medicines Regulations 2012 (“the Regulations”). The MHRA carries out a number of activities in this regard including the routine scrutiny of promotional material for medicinal products.

MHRA requested that the detail aid and leave piece along with supporting references were submitted for scrutiny.

MHRA had no objection to the promotional materials submitted and had no further comments.