There are three critical areas where companies most often go wrong: data preparation and training, choosing tools and specialists and timing and planning.

Objective To assess whether post-authorisation studies registered with the European Medicines Agency (EMA) adhere to legislation and recommendations to publicly post study protocols and results.

Derek Woodcock gives an overview of the Pharmacovigilance System Master File in our safety and pharmacovigilance themed month. The requirement for a Pharmacovigilance System Master File (PSMF) has ...

The national mood is somewhere between anxiety, resignation and anticipation as President Trump considers whether to attack Iran. By Aaron Boxerman President Trump has kept up a steady drumbeat of ...