Clinical trial sponsors looking to stay at the forefront of efficiency and accuracy should consider whether they are making the best use of the growing trend of access to clinical data on mobile devices. From the secure sharing of electronic patient reported outcome (ePRO) data, to creating more flexible clinical data management, mobile technology has the potential to improve processes across the clinical research process. Read more.
Optimizing Clinical Trial Enrollment
Potential clinical trial participants and sponsors typically wait 2 to 3 days for lab results to determine eligibility. For the would-be participant, every day that elapses could contribute to the loss of interest and increases the risk of losing a potential study subject for many reasons. Read more.
ExL Pharma’s eClinical Trial Management Summit will assist you in developing a clear understanding of a fully-integrated eClinical system through industry case studies and best practices. Additionally, this two-day program will enable you to gain valuable strategies for increasing your data monitoring abilities by developing a data management system that integrates the needs of the sponsor, CRO, and vendors.
Martin Harvey, head of communications at the European Medicines Agency (EMA) and EU advisor to the DIA 2012 annual meeting program committee, explains not only what he hopes to learn from attending sessions and walking the DIA exhibit floor, but provides insight into how global changes over the past 12 months have shaped this year's annual meeting's program.
LogPad: Trusted By Sponsors For Over Ten Years
As the voice of the patient becomes increasingly relevant in drug approvals, trial sponsors need new and better ways to collect and manage PRO data. The PHT LogPad System is the most trusted ePRO solution, used in clinical trials around the world. Read more.
Clinical Technology Services From ICON
ICON develops, implements, and manages interactive voice and Web response systems (IVRS and IWRS), along with cutting-edge Web technology, to increase the accuracy and efficiency of conducting global clinical studies. Read more.