Jean Paty, Ph.D. – Founder and Senior Vice President, Scientific, Quality and Regulatory Affairs

Jean Paty, Ph.D., is Co-founder and Senior Vice President of Scientific, Quality and Regulatory Affairs for invivodata, inc. where he is responsible for working with scientific, technical and clinical operations components of the company to ensure that all aspects of the business meet FDA and international data standards for the pharmaceutical industry.

Dr. Paty has published extensively on the regulations guiding development and implementation of ePRO. He has worked with industry and regulatory agency groups on ePRO best practices, and he has collaborated with invivodata Co-founder Dr. Saul Shiffman since 1990 on the development of real-time, real-world solutions to study patient experience. Dr. Paty earned his B.S. in Psychology from the University of Toronto and an M.S. and Ph.D. in Psychology from the University of Pittsburgh.

• Meet with Dr. Paty at PROficiency™ 2011  – our international series of regional, 1-day conferences
• Read Dr. Paty’s recent article from Applied Clinical Trials, “Measurement is Strategic”
• Read Dr. Paty’s Closing Thought in Applied Clinical Trials February 2011 edition, “The Patient Matters: A Big Thank you to FDA” 
• Access recordings of Jean’s recently conducted webinars:

Is Your PRO Instrument Ready for Regulatory Inspection?

Interpreting Regulatory Feedback on PRO Instruments:  Now What?