Refining Patient Reported Outcomes
- October 28, 2008
Webinar: ePRO Regulatory Environment in Europe
Are you familiar with the current regulatory environment in Europe with respect to the use of electronic patient reported outcomes? Do you understand the expectations of agencies such as EMEA? Join us for an interactive Web Seminar that will explore various elements to consider for ensuring appropriate regulatory compliance when considering patient reported outcomes in your clinical research.
Presenter: Jean Paty, Ph.D. - Chief Scientist and Regulatory Advisor, PRO Consulting
Download the "ePRO Regulatory Environment in Europe" webinar, which was designed to help researchers make key decisions about their PRO strategy and instruments for clinical programs and individual trials.
