France

Franrenet, S., Moutel, G., Raffi, F., Dabis, F., Bruyand, M., Hervé, C., & … Duchange, N. (2011). Information that should be given to HIV cohort participants during ongoing research: The viewpoints of patient representatives and research professionals. Journal Of Empirical Research On Human Research Ethics, 6(4), 76-83.
Investigator practices and perspectives, Adults (other)People at risk for or living with other STIs, People living with HIV, Clinical trials, Health-care facilities, France, Mixed methods (MM)

Advertisements

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s