Reporting Side Effects

In the complex, globalized world of pharmaceuticals, clear communication is a matter of patient safety. MedDRA (the Medical Dictionary for Regulatory Activities) is the critical, standardized terminology that ensures a "heart attack" in a report from Japan is understood identically by a regulator in Europe. This article explores how this universal language powers...

These are the official bodies in each country where you can report suspected side effects of medicines, vaccines, and quality issues.

EMA GVP