Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

ePharmaSolutions

From Wikipedia, the free encyclopedia
Contract Research Organization and Clinical Research Software Provider
This article has multiple issues. Please helpimprove it or discuss these issues on thetalk page.(Learn how and when to remove these messages)
A major contributor to this article appears to have aclose connection with its subject. It may require cleanup to comply with Wikipedia's content policies, particularlyneutral point of view. Please discuss further on thetalk page.(January 2011) (Learn how and when to remove this message)
icon
This articleneeds additional citations forverification. Please helpimprove this article byadding citations to reliable sources. Unsourced material may be challenged and removed.
Find sources: "EPharmaSolutions" – news ·newspapers ·books ·scholar ·JSTOR
(September 2012) (Learn how and when to remove this message)
(Learn how and when to remove this message)

ePharmaSolutions (ePS), as acontract research organization, is an Americanclinical research provider. The solutions includeproprietary software applications and global clinical services that focus on the major areas of clinical study delays.

ePS was founded in 2001 by Lance Converse and is headquartered in Plymouth Meeting, Pennsylvania, employing 60+ clinical researchers and technologists. ePharmaSolutions' Clinical Trial Portal technology won the 2009 and 2013 Bio-IT World[1] for “Best in Class Clinical Trial Technology” and the 2013 Microsoft Lifesciences Innovation Award[citation needed] making it the most widely used Clinical Trial Portal and Electronic Trial Master File solution[buzzword] in the pharmaceutical industry with over 350,000 users in 130 countries.[2]

Clinical trial software

[edit]
  • Clinical Trial PortalClinical Trial Portal- Single-sign-on application used by more than 300,000 clinical researchers in 130 countries.
  • User Management Application & Vendor Integration Manager - Single sign-on and user provisioning applications for clinical trial technologies
  • Investigator Database - over 300,000 investigators in 120 countries
  • Site Feasibility Application - secure online site feasibility and ranking application
  • Secure Document Exchange - online completion of study documents and contracts withdigital signature
  • Safety Letter Distribution - safety letter distribution and tracking system
  • Learning Management System - delivery and tracking of on and offlinetraining andcertification programs
  • Patient Recruitment Manager - develop and track globalpatient recruitment and retention programs
  • Electronic Monitor Visit Report Application - track all monitor visits using the on or offline capabilities (withelectronic signature)
  • Electronic Trial Master File - tracks the completion and filing of clinical trial documents via configurable workflow and reference models.

Global clinical research services

[edit]
  • Site Feasibility and Selection - Access to over 300,000 investigators profiled by experience and patient populations
  • Site Activation - Secure document exchange technology with site support services
  • Study/Site/Systems Training - Training of clinical research professionals
  • Inter-rater Reliability Services and Data Monitoring - Custom tailored solutions[buzzword] for most every scale, delivered in over 50 countries
  • Patient Recruitment and Retention - Full service solutions[buzzword] supporting programs in over 60 countries

References

[edit]
  1. ^"Trial Portal Tightens Bond with Investigative Sites".Bio IT World. Retrieved24 September 2025.
  2. ^"Clinical trials news".

External links

[edit]
Clinical research
Clinical and healthcare IT
Manufacturing
Portals:
Retrieved from "https://en.wikipedia.org/w/index.php?title=EPharmaSolutions&oldid=1313151007"
Category:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp