Table 2.

Overview of the training activities for clinical research in each country

Training activity	Country
	CZE	FRA	DEU	HUN	IRL	ITA	NOR	PRT	SVK	ESP	CHE
GCP	X	X	X	X	X		X	X	X	X	X
Study nurse/coordinator	X		X	X	X	X	(X)	X	(X)	X	X
Investigator	X	X	X	X	X	X		X	X	X	X
Monitoring	X	X	X	X			X	X		X	X
PV/clinical pharmacology	X		X	X				X	(X)	X	X
Principal investigator	X	X	X	X				X	X		X
CRO operators			X			X		X
Methodology		X			X			X		X	X
QMS	X	X	X		X			X
Postgraduate	X		X	X	X		X	X	X		X
Other		X	X	X	X						X

X = available, (X) = planned

CZE Czech Republic, FRA France, DEU Germany, HUN Hungary, IRL Ireland, ITA Italy, NOR Norway, PRT Portugal, SVK Slovakia, ESP Spain, CHE Switzerland, GCP Good Clinical Practice, PV pharmacovigilance, CRO clinical research organization, QMS quality management system