Table 3. What information should be provided to participants/donors in the IC?

In your opinion, what information should be provided to participants/donors in the IC?		Should be provided in the IC	Is not essential in the IC	I don’t know
The purpose and (future) objectives of the associated research	n	184	32	1
	%	84.8%	14.7%	0.5%
Possibility of re-contact by researchers for additional data/sampling	n	175	41	2
	%	80.3%	18.8%	0.9%
Possibility of returning individual research results	n	150	60	7
	%	69.1%	27.6%	3.2%
Sharing data/samples with other non-commercial research partners	n	194	17	4
	%	90.2%	7.9%	1.9%
Sharing data/samples with commercial and/or health industry partners	n	181	24	11
	%	83.8%	11.1%	5.1%
Sharing data/samples with parties in other EU countries	n	172	36	10
	%	78.9%	16.5%	4.6%
Sharing data/samples with parties in non-EU countries	n	169	39	11
	%	77.2%	17.8%	5.0%