Dear HCP community and developers, In preparing for an upcoming study, one of my collaborators has asked whether the CONNECTOM scanners require any special statements in the informed consent form. The reason behind this is that, from what we understand, CONNECTOM scanners are not standard clinical scanners with CE certification (or other equivalent certification in USA). Being uncertified, the subject will be put in a machine that has not passed certain tests from the authorities. Not sure what those tests are or what is certified in an CE certification, but the logic makes sense.
I wanted to ask whether anybody has encountered this issue before for those of you who have used CONNECTOM scanners or other out-of-series scanners before. I realize this is a highly specialized question not directly pertaining to the HCP user community, but I am hoping that someone may have tips on the issue. Thank you. Dorian _______________________________________________ HCP-Users mailing list [email protected] http://lists.humanconnectome.org/mailman/listinfo/hcp-users
