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I-Tech Project Will Turn Out in Lower Costs for the Clinical Research Arena
Date:10/25/2013

tem in order to allow CROs, investigational sites and PIs gain access to every steps of the regulatory process and document assessment follow up by IEC.

Through this, the most challenging activity in clinical trials will be sorted thanks to a unique dynamic, on line, follow up system, where any inquire or question, can duly be solved giving back the necessary feedback to complete all the requirements in a reliable, faster and efficient way.

Clinical Trial Foundation is also thinking of expanding this novel system to other Clinical Trial steps with a service pack of the same scheme.

“Time is already important and is coming to be called the golden key in clinical trials, it is necessary to work fast and safely, with dependable methods, but all of us know how hard the impact is on the final budget in this field…” said Dr. Uviedo.

We invite every IEC, CRO, Clinical Trial Institutions and Investigational Sites to consider their registration in this service, not only to test what could be a very helpful tool to shorten regulatory timeframes, but also to get into the feeling of accompanying the document assessment live and interacting directly in between with the main decision making persons.

Read the full story at http://www.prweb.com/releases/2013/10/prweb11159460.htm.


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