New Cloud-Based Investigator Portal from Veeva Systems Speeds Clinical Study Start-Up
Poster: SySAdmin
Posted on June 24, 2013 at 6:21:01 AM
New Cloud-Based Investigator Portal from Veeva Systems Speeds Clinical Study Start-Up
BOSTON, June 24, 2013 /PRNewswire/ --
Single source for sponsor, CRO and investigator collaboration
During the Drug Information Association's (DIA) annual meeting today, Veeva Systems
previewed its new Veeva Vault Investigator Portal. As a companion product to Vault eTMF,
Vault Investigator Portal enables fast collection, sharing and tracking of all
investigator content from a single platform. Veeva has specifically designed its new
Investigator Portal to speed study start-up by simplifying the overall trial document
management process and providing bi-directional, direct access to the eTMF.
(Logo:
http://photos.prnewswire.com/prnh/20120425/527164 )
(Photo:
http://photos.prnewswire.com/prnh/20130624/622707 )
Clinical trials are one of the most complex areas of a life sciences company's
operations, requiring global reach, coordination and tracking across multiple
stakeholders. Investigators and site personnel spend hundreds of hours performing
redundant tasks across multiple sponsors and systems. Most trial technologies hinder
investigator efficiency and breed frustration. Veeva's cloud-based Vault Investigator
Portal orchestrates collaboration with site personnel for more efficient operations.
"Without a doubt, the back and forth between investigators and the CRO or sponsor is
causing huge delays in study start-up. Most of these documents are still exchanged as
paper, which is slow and adds expense. Sponsors and CROs must find ways to improve the
efficiency while protecting the increasingly important site relationship," said Michael
Burton, director of clinical product strategy at Veeva.
Veeva's Vault Investigator Portal helps streamline trials and increase efficiency with
features that lessen the workload for sponsors and investigators, including:
- Single source for sponsors, CROs and investigator sites to submit and
access documents
- Direct placement of site documents into the eTMF
- Two-way channel for exchanging documents, including safety alerts and site
training videos
- Prioritised to-do lists and associated documents packaged and pushed to
investigator sites
"With Vault Investigator Portal, sponsors and CROs will benefit from better document
tracking and placement into the eTMF," concluded Burton. "The ease-of-use and efficiency
for investigators will make working with the sponsor and CRO more attractive, which should
keep investigators coming back for trial after trial."
Also announced at DIA 2013 today, Veeva adds critical publishing capabilities to Vault
Submissions - the industry's first cloud-based application for managing submissions
content.
About Veeva Vault Development Suite
Vault Investigator Portal is part of the Veeva Development Suite, the only cloud-based
suite of integrated content management applications for the life sciences industry.
Spanning every major part of a life sciences company - from R&D to clinical trials, to
quality and manufacturing - the Veeva Development Suite gives pharmaceutical,
biotechnology and medical device companies the ability to deploy a single content
management system globally. All Development Suite applications offer real-time reporting
and dashboards, an intuitive web interface, and a true multitenant cloud architecture that
continuously delivers rapid innovation.
About Veeva Systems
Veeva Systems is a leader in cloud-based software for the global life sciences industry.
Committed to innovation, product excellence and customer success, Veeva has over 150
customers, ranging from the world's largest pharmaceutical companies to emerging biotechs.
Founded in 2007, Veeva is a privately held company headquartered in the San Francisco Bay
Area, with offices in Philadelphia, Barcelona, Budapest, London, Paris, Beijing, Shanghai
and Tokyo. For more information, visit http://www.veeva.com.
Media Contact
Lisa Barbadora
Veeva Systems, Inc.
pr@veevasystems.com
Copyright (c) 2013 Veeva Systems. All rights reserved. Veeva and the Veeva logo are
registered trademarks of Veeva Systems. Veeva Systems owns other registered and
unregistered trademarks. Other names used herein may be trademarks of their respective
owners.
Photo:
http://photos.prnewswire.com/prnh/20120425/527164
http://photos.prnewswire.com/prnh/20130624/622707
Photo:http://photos.prnewswire.com/prnh/20120425/527164
http://photoarchive.ap.org/
Photo:http://photos.prnewswire.com/prnh/20130624/622707
http://photoarchive.ap.org/
Veeva Systems
CONTACT: +1-610-420-3413
BOSTON, June 24, 2013 /PRNewswire/ --
Single source for sponsor, CRO and investigator collaboration
During the Drug Information Association's (DIA) annual meeting today, Veeva Systems
previewed its new Veeva Vault Investigator Portal. As a companion product to Vault eTMF,
Vault Investigator Portal enables fast collection, sharing and tracking of all
investigator content from a single platform. Veeva has specifically designed its new
Investigator Portal to speed study start-up by simplifying the overall trial document
management process and providing bi-directional, direct access to the eTMF.
(Logo:
http://photos.prnewswire.com/prnh/20120425/527164 )
(Photo:
http://photos.prnewswire.com/prnh/20130624/622707 )
Clinical trials are one of the most complex areas of a life sciences company's
operations, requiring global reach, coordination and tracking across multiple
stakeholders. Investigators and site personnel spend hundreds of hours performing
redundant tasks across multiple sponsors and systems. Most trial technologies hinder
investigator efficiency and breed frustration. Veeva's cloud-based Vault Investigator
Portal orchestrates collaboration with site personnel for more efficient operations.
"Without a doubt, the back and forth between investigators and the CRO or sponsor is
causing huge delays in study start-up. Most of these documents are still exchanged as
paper, which is slow and adds expense. Sponsors and CROs must find ways to improve the
efficiency while protecting the increasingly important site relationship," said Michael
Burton, director of clinical product strategy at Veeva.
Veeva's Vault Investigator Portal helps streamline trials and increase efficiency with
features that lessen the workload for sponsors and investigators, including:
- Single source for sponsors, CROs and investigator sites to submit and
access documents
- Direct placement of site documents into the eTMF
- Two-way channel for exchanging documents, including safety alerts and site
training videos
- Prioritised to-do lists and associated documents packaged and pushed to
investigator sites
"With Vault Investigator Portal, sponsors and CROs will benefit from better document
tracking and placement into the eTMF," concluded Burton. "The ease-of-use and efficiency
for investigators will make working with the sponsor and CRO more attractive, which should
keep investigators coming back for trial after trial."
Also announced at DIA 2013 today, Veeva adds critical publishing capabilities to Vault
Submissions - the industry's first cloud-based application for managing submissions
content.
About Veeva Vault Development Suite
Vault Investigator Portal is part of the Veeva Development Suite, the only cloud-based
suite of integrated content management applications for the life sciences industry.
Spanning every major part of a life sciences company - from R&D to clinical trials, to
quality and manufacturing - the Veeva Development Suite gives pharmaceutical,
biotechnology and medical device companies the ability to deploy a single content
management system globally. All Development Suite applications offer real-time reporting
and dashboards, an intuitive web interface, and a true multitenant cloud architecture that
continuously delivers rapid innovation.
About Veeva Systems
Veeva Systems is a leader in cloud-based software for the global life sciences industry.
Committed to innovation, product excellence and customer success, Veeva has over 150
customers, ranging from the world's largest pharmaceutical companies to emerging biotechs.
Founded in 2007, Veeva is a privately held company headquartered in the San Francisco Bay
Area, with offices in Philadelphia, Barcelona, Budapest, London, Paris, Beijing, Shanghai
and Tokyo. For more information, visit http://www.veeva.com.
Media Contact
Lisa Barbadora
Veeva Systems, Inc.
pr@veevasystems.com
Copyright (c) 2013 Veeva Systems. All rights reserved. Veeva and the Veeva logo are
registered trademarks of Veeva Systems. Veeva Systems owns other registered and
unregistered trademarks. Other names used herein may be trademarks of their respective
owners.
Photo:
http://photos.prnewswire.com/prnh/20120425/527164
http://photos.prnewswire.com/prnh/20130624/622707
Photo:http://photos.prnewswire.com/prnh/20120425/527164
http://photoarchive.ap.org/
Photo:http://photos.prnewswire.com/prnh/20130624/622707
http://photoarchive.ap.org/
Veeva Systems
CONTACT: +1-610-420-3413