Clinical Research Software allows online and offline reporting.
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Press Release Summary:
Electronic Monitor Visit Report (eMVR) v3.0 allows study monitors to complete their site visit reports either online or offline in Microsoft Word for later submittal back to eMVR. The eMVR auto-populates visit reports, confirmation and follow-up letters, and carries all follow-up data from one report to either follow-up letters or future visit reports. It also integrates with leading CTMS systems.
Original Press Release:
ePharmaSolutions Launches New Version of Electronic Monitor Visit Report Application with Industry-Leading Online and Offline Capabilities
CONSHOHOCKEN, Pa. - ePharmaSolutions, a leading provider of clinical research technologies and niche clinical services, launches version 3.0 of its eMVR (Electronic Monitor Visit Report) application with new features to support online and offline completion of monitoring reports for traveling clinical research associates and integrations with leading CTMS systems.
"Our latest release provides study monitors with the option of completing monitor reports online or offline, more robust reporting, and CTMS integration points," stated Steven Beales, ePharmaSolutions' Vice President of Information Technology.
ePharmaSolutions' Clinical Trial Portal (CTP) is used by more than 200,000 clinical researchers in 107 countries to help accelerate and improve site feasibility, study training, site activation and patient enrollment. CTP version 4.0 contains new functionality for sponsors that includes eMVR (Electronic Monitor Visit Report) to support the authoring, completion and submission of online and offline monitor trip reports with electronic signature. The new version of eMVR allows study monitors to complete their site visit reports online or offline in Microsoft Word. The offline reports can be submitted back to the eMVR and the data is pulled from the Word template back into the system. The eMVR auto-populates visit reports, confirmation and follow-up letters, and carries all follow-up data from one report to either follow-up letters or future visit reports. The eMVR includes a robust tracking and reporting system for study managers and integrates with leading CTMS systems.
"Our clients have been asking for an offline monitor visit report completion feature for some time and the market has not been responding in a timely enough manner," stated Lance Converse, ePharmaSolutions' Founder and CEO. "Our development team did an excellent job building out these features into this release to support the global needs of our biopharmaceutical and CRO clients," Converse added.
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). Future plans in 2010 include the inclusion of a grant payment tracking application for sponsors/sites and integration of 80 million EMR records into its investigator database for improved decision support during the site selection process.
About ePharmaSolutions, Inc.
ePharmaSolutions is a leading provider of technology-based clinical services that help improve the way sites are selected, trained, activated and supported to start clinical trials and meet enrollment goals. ePharmaSolutions has activated and trained more than 185,000 clinical researchers in 107 countries for the top 20 pharmaceutical companies in the world and is headquartered in Philadelphia, Pennsylvania. For more information call 610-832-9915 or visit www.epharmasolutions.com.
Source: ePharmaSolutions
CONTACT: Lance Converse of ePharmaSolutions, +1-610-832-9915
Web Site: www.epharmasolutions.com/
