Please plan to visit us at the ARVO 2014 Annual Meeting and Conference in Orlando, FL on May 4-8 . We’ll be located in booth number 741. Sterling’s study start-up team and board members have extensive experience in reviewing protocols for ophthalmic clinical trials. For investigator initiated studies, Sterling can assist you in formalizing a study plan that will meet regulatory approval criteria. If you’d like to schedule a meeting to discuss our services and capabilities, please contact Kathye Richards, CIP, Director of Client Services at 678-501-7806 or kathye.richards@sterlingirb.com. We look forward to seeing you at ARVO.