invivodata inc., the industry leader in electronic patient reported outcomes (ePRO) solutions and services for global clinical research, today announced its 2009 ePROficiency Web seminar series on Patient Reported Outcomes (PRO).
The webinar series is a continuation of invivodata’s educational initiative which focuses on recent regulatory and industry trends related to PROs. Each of the series’ webinars is derived from presentations that were delivered by industry experts during invivodata’s ePROficiency Conference in Naples, FL.
Each complimentary webinar will feature international pharmaceutical researchers delivering insight on specific aspects of PRO in clinical research and answering questions on topics including:
Developing PROs: Common Pitfalls & Recent Experiences – September 10
Supporting Regulatory Submissions and Inspections: the ePRO Perspective – October 22
eDiaries: From Clinical Proof-of-Concept through to NDA Approval – December 3
“We’ve always been very pleased with the response to our webinar programs, which represents the growing interest we’ve seen in PROs for clinical research,” said Dr. Jean Paty, chief scientist and regulatory advisor at invivodata’s consulting division, PRO Consulting. Considering the evolving use of PROs and its regulatory implications, it’s no surprise that so many global trial sponsors are eager to learn more about the latest PRO strategies and trends.”
Date: June 9, 2009
Source: invivodata inc.
Filed Under: Drug Discovery
