EU moves toward web portals for adverse events

The European Parliament has signed off on the Pharmacovigilance directive, which would require national governments to set up medicine web portals containing information on drug products and side effects. Instructions for reporting suspected adverse reactions would also be included. Article

Suggested Articles

There's no evidence personal patient information leaked during the 11-week breach, but the same can't be said about Sangamo's own secrets.

Through a new online tracker, AllTrials names sponsors who fail to report clinical trial results on time per the FDAAA Final Rule.

The new solution aims to streamline the incorporation of human genomic data into clinical trial designs.