ARTClinica Launches the Most Cost-Effective Robust Scalable Customizable eClinical Software Solution
ARTClinica introduces its new eClinical software solution. The solution will be demonstrated at the Partnerships in Partnerships in Clinical Trials Conference taking place on March 30 – April 1 in Phoenix, AZ.
Cherry Hill, NJ, March 18, 2011 --(PR.com)-- ARTClinica proudly introduces its same-name software solution, which is the most cost-effective robust scalable customizable solution combining Electronic Data Capture (EDC), Clinical Trial Management (CTMS) with optional Interactive Voice/Web Response Software (IVRS/ IWRS) into a single integrated system for a fraction of the cost of other custom-made solutions.
The ARTClinica solution is intended to support bio-pharma companies with a need for a lightweight integrated eClinical solution; CROs managing studies of any sizes; independent clinics; pharmaceutical companies collaborating on a study and imaging labs. The solution significantly decreases the number of errors that appear when using huge amounts of manually filled paper-documents, forms and Excel datasheets during a trial. All this in a robust SaaS model enabling the subscriber to only pay for what they use and only while they are running their trials with no license fees or IT capital investments.
Sina Adibi, General Manager: “ARTClinica offers a new approach in technology applications integration for use in clinical trials. By building tight integration between IVR/ IWR and EDC, we have effectively combined EDC-IVR capabilities in such a way that IVR is just another interface to our robust web-based EDC. Our role-based workflow environment allows for speedy study protocol configuration and site setup, easy electronic case report form composition (eCRFs), enabling study managers to effectively collect data and manage trials securely.”
Site users can enter data in real time through the EDC or IVRS with no possibility of conflict. Users can conveniently use web and voice to best perform their daily activities without the need to synchronize data. These advanced capabilities achieve true interoperability and mean users and administrators benefit from significantly simplified workflow, saving time and effort during setup and while using the system. As everything is entered into a single store there is no need to move data from one system to another.
Additionally, ARTClinica’s development, validation and support team (24/7 help desk) with many years of experience in developing study management tools stand at the ready to assure fastest ramp-up time and technology training of client’s teams. As standard practice, a dedicated IT project manager will coordinate all setup as well as ongoing systems activities.
It's also worth mentioning that ARTClinica is developed with the financial backing of the LANIT group, which is a $1.1 billion IT Services vendor with over 4,000 employees.
ARTClinica will be first time demonstrated to the public at the Partnerships in Clinical Trials conference at booth #626. The event will take place at the Phoenix Convention Center, AZ on March 30 – April 1, 2011.
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The ARTClinica solution is intended to support bio-pharma companies with a need for a lightweight integrated eClinical solution; CROs managing studies of any sizes; independent clinics; pharmaceutical companies collaborating on a study and imaging labs. The solution significantly decreases the number of errors that appear when using huge amounts of manually filled paper-documents, forms and Excel datasheets during a trial. All this in a robust SaaS model enabling the subscriber to only pay for what they use and only while they are running their trials with no license fees or IT capital investments.
Sina Adibi, General Manager: “ARTClinica offers a new approach in technology applications integration for use in clinical trials. By building tight integration between IVR/ IWR and EDC, we have effectively combined EDC-IVR capabilities in such a way that IVR is just another interface to our robust web-based EDC. Our role-based workflow environment allows for speedy study protocol configuration and site setup, easy electronic case report form composition (eCRFs), enabling study managers to effectively collect data and manage trials securely.”
Site users can enter data in real time through the EDC or IVRS with no possibility of conflict. Users can conveniently use web and voice to best perform their daily activities without the need to synchronize data. These advanced capabilities achieve true interoperability and mean users and administrators benefit from significantly simplified workflow, saving time and effort during setup and while using the system. As everything is entered into a single store there is no need to move data from one system to another.
Additionally, ARTClinica’s development, validation and support team (24/7 help desk) with many years of experience in developing study management tools stand at the ready to assure fastest ramp-up time and technology training of client’s teams. As standard practice, a dedicated IT project manager will coordinate all setup as well as ongoing systems activities.
It's also worth mentioning that ARTClinica is developed with the financial backing of the LANIT group, which is a $1.1 billion IT Services vendor with over 4,000 employees.
ARTClinica will be first time demonstrated to the public at the Partnerships in Clinical Trials conference at booth #626. The event will take place at the Phoenix Convention Center, AZ on March 30 – April 1, 2011.
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Contact
ARTClinica
Oleg Yudin
+1 856 452-0864
www.art-clinica.com
Oleg Yudin
+1 856 452-0864
www.art-clinica.com
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