ClinPhone Showcases its Combined EDC-IVR Solution and Complete Range of Clinical Technology Solutions at DIA’s 44th Annual Meeting
(Nottingham UK, 15 April 2008). ClinPhone, the world’s largest Clinical Technology Organization (CTO), will be showcasing its combined EDC-IVR solution and its comprehensive portfolio of clinical technology solutions at booth #217 at DIA’s 44th Annual Meeting, June 22-26, 2008 in Boston, MA.
ClinPhone’s combined EDC-IVR offering brings together two industry-leading solutions, DataLabs by ClinPhone (EDC) and ClinPhone Randomization and Trial Supply Management (IVR/IWR), into one integrated solution. In-booth discussions and demonstrations will be offered to showcase the power of this innovative solution.
In addition to showcasing its combined EDC-IVR solution, ClinPhone will be demonstrating its complete portfolio of clinical technology solutions, including electronic data capture (EDC), randomization, trial supply management, drug accountability, electronic patient reported outcomes (ePRO), clinical trial management systems (CTMS) and integration solutions. ClinPhone is the first company of its kind to offer such a comprehensive suite of software and services to the biopharmaceutical industry.
Members of ClinPhone will be presenting at several sessions during the event. Industry hot topics covered during ClinPhone’s sessions* include maximizing EDC potential, adaptive trial design, trial supply management and electronic patient reported outcomes (ePRO) validation.
DIA’s Annual Meeting is the largest biopharmaceutical industry event, drawing over 5,000 industry professionals each year and over 450 exhibiting companies from around the world. Additionally, DIA’s Annual Meeting provides over 350 conference sessions covering 26 content tracks and numerous networking opportunities.
For further information on ClinPhone’s clinical technology solutions, please visit booth #217 at DIA’s 44th Annual Meeting in Boston. Alternatively, please visit www.clinphone.com or e-mail info@clinphone.com.
*Speaking sessions include:
Monday, June 23, 2008
Time: 10:30 a.m. – 12:00 p.m.
Session: Adaptive Design in Clinical Research
Presentation: Great Adaptations: A Novel Approach to Clinical Study Design
Speaker: Graham Nicholls, MS, Product Manager
Time: 3:30 p.m. – 5:00 p.m.
Session: An Honest Look at the eClinical Process: How Biotechnology Can Learn from Best Practices Outside the Industry
Presentation: Back to EDC Basics: Things You Need to Know to Maximize Your EDC Potential
Speaker: Paula McHale, Product Management Director, Data Management
Solutions
Tuesday, June 24, 2008
Time: 2:00 p.m. – 3:30 p.m.
Session: Good Practices for Clinical Endpoint (PRO, CRO) and Linguistic Validation: State of the Science
Presentation: Quantitative Validation of PROs and CROs
Speaker: Keith Wenzel, Product Director, ePRO
Time: 2:00 p.m. – 3:30 p.m.
Session: Solving Complex Problems in Clinical Trial Supply Management
Presentation: Estimating Medication Requirements for Adaptive Trial Designs
Speaker: Bill Byrom, Ph.D., V.P. Product Strategy and Marketing (session chair and speaker)
Wednesday, June 25, 2008
Time: 8:30 a.m. – 10:00 a.m.
Session: Anatomy of ePRO Validation
Presentation: Psychometric Validation for Electronic Patient Reported Outcomes
Speaker: James Pierce, Ph.D., ePRO Partnering Manager
Keith Wenzel, Product Director, ePRO (session chair)
Time: 1:30 p.m. – 3:00 p.m.
Session: Planning, Analysis, and Review of Clinical Trials: Selected Topics
Presentation: Validation of Modified PRO Instruments: The State of the Statistical Science
Speaker: Damian McEntegart, MS, V.P. of Statistics and Product Support Services
