DATATRAK International, Inc. : DATATRAK Releases New Version of uIRT
January 18, 2012 at 07:25 pm IST
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Empowering Clients with Control of Randomization and
Inventory in the Cloud
CLEVELAND, [January 18th] /PRNewswire/ - DATATRAK
International, Inc. (OTCQX: DATA), a technology and
services company focused on global eClinical solutions for
the clinical trials industry, today announced a completely
new product design for their randomization and clinical
supplies management product, uIRT. As a unified product
within the DATATRAK ONE™ suite, the new release of uIRT
positions DATATRAK as the most advanced unified
Randomization and Clinical Supplies Management system in
the marketplace today.
"DATATRAK has been supporting clinical trial randomizations
and drug inventory management since 2005," stated DATATRAK
CTO Chris Wilke. "With this new release, we've made huge
strides in the technologies available to the marketplace
today. We listened to our clients and have now turned over
the control of managing trial randomizations to Sponsors
and CROs."
Clients can configure and maintain randomization and
clinical supply allocation throughout the life of the
clinical trial without DATATRAK assistance. With this new
release, users will experience the following:
Increased performance when generating randomization
schedules, importing strata and populating or importing
inventory schedules.
Robust Manager functionality allowing users to view,
filter, update and export information on drug containers,
drug assignments, shipments and randomization schedules.
Standard reports and system-wide exports available 24/7
in real-time to effectively manage time sensitive
randomization and inventory needs.
About DATATRAK
DATATRAK International is a worldwide technology and
services company delivering eClinical solutions and related
services for the clinical trials industry. DATATRAK built
its multi-component, comprehensive solution on a single,
unified platform and expanded this concept to include
services delivery via DATATRAK's Clinical and Consulting
Services™ group. The Company delivers a complete portfolio
of software products designed to accelerate the reporting
of clinical research data from sites to sponsors and
ultimately regulatory authorities, faster and more
efficiently than loosely integrated technologies. The
DATATRAK ONE™ software solution, deployed worldwide through
an ASP or Enterprise Transfer offering, supports Phase I -
Phase IV drug and devices studies in multiple languages
throughout the world. DATATRAK has offices located in
Cleveland, Ohio; Bryan, Texas; and Cary (RTP), North
Carolina. For more information, visit .
Except for the historical information contained in this
press release, the statements made in this release are
forward-looking statements. These forward-looking
statements are made based on management's expectations,
assumptions, estimates and current beliefs concerning the
operations, future results and prospects of the Company and
are subject to uncertainties and factors which are
difficult to predict and, in many instances, are beyond the
control of the Company, and which could cause actual
results to differ materially from those contemplated in
these forward-looking statements. For a list of certain of
the factors that may cause actual results to differ
materially from those contemplated in these forward looking
statements, please see the Company's quarterly report filed
with the OTCQX Market announcing its results for the
three-month period ending September 30, 2011. The Company
undertakes no obligation to update publicly or revise any
forward-looking statement whether as a result of new
information, future events or otherwise.
CONTACT:
Lisa Pahl, Director Marketing, DATATRAK International,
Inc., +1-979-393-9025
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Datatrak International, Inc. is a technology and services company. The Company is engaged in delivering global eClinical solutions for the clinical trials industry. The Company is focused on providing subscription and professional services. Its enterprise platforms include Decentralized Trials (including, electronic consent (e-Consent), electronic patient reported outcomes (e-PRO) and electronic clinical outcomes assessment (e-COA), electronic data capture, clinical trial management system (CTMS) and imaging and endpoint adjudication, randomization, and business intelligence. The Companyâs CTMS includes functions for site feasibility and the tracking of action items and milestones. Its imaging and endpoint adjudication is a streamline the approach for managing imaging components while reducing manual workload and errors. Its business intelligence offers solution to create, monitor, and analyze user research and providing insights that allow to optimize processes from all aspects.