Refining Patient Reported Outcomes
Our Team
Clinical Trial Consultants and Scientific Experts in PRO Methods and Measurements
The scientists of PRO Consulting have more than 140 collective years experience capturing and reporting patient reported outcomes (PRO) data to support drug and medical device development programs worldwide. Our experience includes consulting on more than 270 U.S. and international clinical trials, including participation in Scientific Advisory Boards for a variety of biotechnology and pharmaceutical companies.
Our clinical trial consultants also have extensive experience with the FDA, EMA (formerly EMEA) and other regulatory bodies. The FDA has repeatedly invited our consultants to present to CDER reviewers regarding PRO data and their role in the drug and medical device development process.
PRO Consulting has the most complete and diverse team of scientists experienced in the area of patient reported outcome (PRO) methods and measurements.
Saul Shiffman, Ph.D. – Senior Scientific Consultant
Arthur Stone, Ph.D. – Senior Scientific Consultant
Brian Tiplady, Ph.D. – Senior Scientific Consultant
Scientists & Scientific Consultants
Celeste Elash, M.S. – Scientific Consultant