End of Study Data: Best Practices
- Whose data is it anyway – site or sponsor? If it’s the site’s data, should all the data be sent to the site?
- Best practice for audit trails
- Practical considerations for end of study data transfers, archival and closure processes
Aloft Boston Seaport District, Boston, Massachusetts
Day 1 Tuesday, October 17th @ 2:00-2:45pm EST
Vice President, Scientific E-tech Enabled Services, Calyx
Craig Mooney has nearly 30 years’ experience in the clinical development industry, with concentrated focus on optimizing IRT to improve clinical trial efficiencies. Craig brings a unique understanding of IRT from both a delivery and user perspective, having served as the Director of IRT at Bristol-Myers Squibb for most of the past decade and having held roles in clinical operations, IMP packaging, and labeling & logistics. He is considered an industry expert and has been a featured speaker at numerous IRT conferences including positions as Conference Chairman.