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news.ePharmaSolutions, a provider of clinical research technologies and niche clinical services, has launched Version 4.0 of Clinical Trial Portal Solution with new functionality and additional workflow to support global enterprise implementations.
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ePharmaSolutions’ Clinical Trial Portal (CTP) provides biopharmaceutical companies and CROs with a fully validated solution to help accelerate and improve study start-up and site management through a variety of ‘Site Friendly’ components that include: site feasibility application (SFA), secure document exchange (SDE), safety letter distribution (SLD), electronic monitor visit reporting (eMVR), learning management system (LMS), and the patient recruitment manager (PRM).
Version 4.0 includes new functionality such as eMVR (Electronic Monitor Visit Report) to support the authoring, completion and submission of on and offline monitor trip reports with electronic signature, an improved SFA (Site Feasibility Application) with self-service access to over 200,000 clinical investigators in 127 countries, and the PRM (Patient Recruitment Manager) solution that integrates an IRB/EC material management application with an on demand ordering/tracking feature for global studies.
Steven Beales, vice president of information technology at ePharmaSolutions, said: We have also made significant progress integrating with some of the CTMS and IVRS vendors to implement single-sign-on and ensure a two-way transfer of data can be completed with little, if any, data discrepancy errors between the systems.”