(a) Informed written consent shall be obtained from each client in a research project as follows:
- (1) documentation that the client has been informed of any potential dangers that may exist, and that he understands the conditions of participation; and
- (2) notice of the client's right to terminate participation at any time without prejudicing the treatment he is receiving.
- (b) A copy of the dated, signed consent form shall be kept on file.
History Note: Authority G.S. 148‑19(d);
Eff. January 4, 1994;
Pursuant to G.S. 150B-21.3A, rule is necessary without substantive public interest Eff. June 20, 2015.