The US Food and Drug Administration has published non-mandatory new draft guidance on direct-to-consumer drug advertising, which includes criticism of distracting images or music.
Other elements of the document issued by the agency's Center for Drug Evaluation and Research include using the same typeface for the text for a product's negative features as for its benefits and not speeding up voice-over comments when listing side effects.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze