Execution, integrity, and provenance determine PDF safety.
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.
What to pay attention to, the kinds of schedules to follow, and what you don’t need to worry about at all. Credit...Aart-jan Venema Supported by By Melinda Wenner Moyer This guide was originally ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results