Webinars
Update on CDISC activities from the European Interchange
May 22, 2012. 11 A.M. ET
| Speaker for this Event: | Jennifer Price – Director, Clinical Solutions |
Jennifer will update the audience on CDISC Strategy, CDISC Strategic Goals, Collaborations and development of Therapeutic Area Standards. Information will be based on a private Q&A session with CDISC board members, CDISC operations leadership and Interchange plenary session speakers (e.g. FDA, C-Path, ISO) and from sessions on EHR integration, CDISC SHARE, CDASH and SDTM updates.
Site Monitoring Made Easier
May 31, 2012. 2 P.M. ET
| Speaker for this Event: | Jeremiah Rehm – Clinical Solutions Specialist |
Site Monitoring is a complex process often requiring double data entry into multiple, overlapping systems. These manual, repetitive activities greatly reduce the important time spent at clinical sites with investigators and other site personnel. In addition, Site Visit Reports are typically unconnected with CTMS and it can be very difficult to consolidate this valuable information into meaningful reports and performance metrics. This session will focus on site monitoring challenges, connecting the environment, using Microsoft SharePoint and Outlook, offline data entry, site visit report templates, tracking and measuring performance, as well as providing several real world examples.
The Capabilities of SharePoint for Clinical Trial Operations
June 5, 2012. 1 P.M. ET
| Speaker for this Event: | Les Jordan, CTO - Life Sciences Industry Unit Microsoft |
| Jeremiah Rehm – Clinical Solutions Specialist |
Les Jordan, CTO, Life Sciences Industry Unit at Microsoft, will explain how SharePoint helps companies to manage their clinical operational data, to collect more timely information, and to make more informed decisions.
Jeremiah Rehm, eClinical solutions specialist for BioClinica, will focus on specific benefits that life sciences companies have realized by surfacing clinical operations data from CTMS through SharePoint, and how they extend access to Microsoft Office applications for improved data visibility and control.
The New FDA Draft Guidances – What it means to me as a Site, a CRA and a Data Manager
On-Demand Webcast
| Speakers for this Event: | Jonathan Andrus – Vice President, Data Management and Quality |
The FDA has recently issued draft guidances for Industry on Standards for Clinical eSource and Risk-Based Approaches to monitoring which have a broad impact on almost all facets of the clinical trial management. This webinar series will discuss the impact of recent FDA guidances on industry and approaches to prepare to implement new strategies.
Leveraging SharePoint to Maximize CTMS Adoption and Flexibility
On-Demand Webcast
| Speakers for this Event: | Les Jordan, CTO - Life Sciences Industry Unit Microsoft |
| Bob Leonard, Chief Information Officer - Harvard Clinical Research Institute |