ABSTRACT
On <date>, the <name of Board> approved the protocol entitled <full name of study protocol (version #- dated: xx/xx/xx)> and the accompanying informed consent form (version #- dated: xx/xx/xx)>. The Board also approved the patient diary (version #- dated: xx/xx/xx) and the advertisement <title(version #- dated: xx/xx/xx)>. These approvals expire <in one year> and a continuing review of the research must be accomplished by (xx/xx/xx).
