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International Clinical Trials

The Connected CTMS

Data management is just as critical to the success of a clinical
trial as recruiting the right patients and monitoring risks.
A powerhouse clinical trial management system (CTMS) can
be seen as a valuable addition to a study’s team – one that
brings unrivalled cost savings and efficiencies to the table.

As today’s trials grow in scope, geographical reach and
complexity, outdated management processes are no longer
equipped to handle the vast amount of data being produced
on a daily, if not hourly, basis. Imagine going through the
checkout line at the supermarket and, instead of watching
the cashier electronically scan each product, you must wait
patiently as each individual barcode is read and recorded
manually. Not only is this approach time-consuming, but
it also introduces the potential for human error.

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Brion Regan has nearly 15 years of industry experience and has established himself as a thought leader in the application of data-driven process optimisation and cloud-based technologies that improve clinical development in the clinical research space. As Product Manager for ERT’s Trial Oversight Suite, he leads the commercial development and management of the company’s growing portfolio of Softwareas- a-Service solutions.
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Brion Regan
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News and Press Releases

Charles River Laboratories Acquires KWS BioTest

WILMINGTON, Mass.--(BUSINESS WIRE)--Jan. 11, 2018-- Charles River Laboratories International, Inc. (NYSE: CRL) today announced that it has acquired KWS BioTest, a leading contract research organization (CRO) specializing in in vitro and in vivo discovery testing services for immuno-oncology and inflammatory and infectious diseases. The addition of KWS enhances Charles River’s discovery expertise, with complementary offerings that provide our clients with additional tools in the active therapeutic research areas of oncology and immunology.
More info >>

White Papers

Soothing the Logistical Headache of Clinical Trials

Equilibrium Travel Management

As many as 30 per cent of subjects on phase three clinical studies drop out.  Gruelling schedules, high travel costs and time waiting for expense reimbursement can all be factors in these fall rates, and this can be very problematic, delaying or even leading to the cancellation of the trial.  It is crucial to keep subjects motivated, and through efficient travel and expense management, this can be achieved.
More info >>

 
Industry Events

Outsourcing in Clinical Trials Southeast 2018

13-14 March 2018, Durham, North Carolina

This year’s Outsourcing in Clinical Trials event builds on last year’s incredibly successful conference which will once again be returning to North Carolina with the aim of supporting trial sponsors and solution providers in the RTP and neighboring regions, ensuring trials are delivered on time and partnerships are bettered.
More info >>

 

 

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