The review process of Ohio Clinical Trials begins when a pharmaceutical sponsor submits a draft or final protocol. Dr. Apseloff and his staff then write the consent form, advertisements, recruitment scripts, and chronological flow sheet to facilitate the conduct of the study. They also generate source documents tailored to the specific needs of each individual protocol, and they can create paper case report forms or use electronic data capture. For draft protocols, Dr. Apseloff provides rapid and detailed critiques at no charge. The turnaround time from receipt of a protocol to completion of all documents necessary for IRB review is typically one to two days. Ohio Clinical Trials can use any IRB but have extensive experience with Western IRB and typically receives approved finalized documents within one week of submission.