We are aware of an issue causing the title of some ARTG entries to disappear. We are investigating as a priority and hope to have this resolved as soon as possible.
This Post Market Review Compliance Dashboard User Guide provides step-by-step instructions on how to respond to a medical device post-market review notification from the Therapeutic Goods Administration (TGA) through the Post Market Review (PMR) compliance dashboard.
The dashboard is designed to allow sponsors to view any requests or notifications from the TGA, and to respond to them.