Our research organization, The Institute for Quality Resource Management, has a proven track record in
helping manufacturers plan, design protocols, enroll patients, and direct clinical trials for new
medical products. We have devised a method to collect relevant cost and outcome data during the
process of your clinical trial. This process, if undertaken concurrently with Phase III clinical
trials, can enhance your product’s time to market with improved financial success. Data gathered
during the clinical trial phase can help derive our cost effectiveness formulas.
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