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Since 1985 Ness Technologies has been providing leading-edge IT solutions and services to Life Sciences companies around the world. From large pharmaceutical companies to biotechnology, biopharmaceutical and contract research organizations, Ness provides true value to its clients by leveraging unrivaled industry expertise and deep technology skills enabling clients to decrease time-to-market and improve operational excellence. Ness partners with industry leading technology providers to create solutions customized to your organization’s unique requirements. Using our global delivery capabilities Ness can help you develop global solutions that meet your strategic and economic objectives.
We enable life sciences companies to attain sustainable competitive advantage in meeting their requirements to:
Continuously develop new products
Enhance R&D and clinical trial efficiencies
Globally manage projects and leverage assets
Maintain cost-effective compliance with all regulatory agencies
We provide innovative clinical trial management solutions in these areas:
Clinical Trial Support: End-to-end solutions for life sciences firms that lack the resources to develop these capabilities in-house.
Electronic Data Capture (EDC)
Clinical Trial Management Solutions (CTMS)
Clinical Trial Data Management and Data Security
Regulatory Affairs Support Services: Helping clients ensure regulatory compliance for submissions and data management within the enterprise:
EMC Documentum Systems Architecture, Development and Support
Standard Operating Procedure (SOP) Development
Global Electronic Submissions BPR
Common Technical Document (CTD) and e-CTD Architecture, Design and Implementation
In addition, we provide clients with the ability to architect and implement robust enterprise content & document management solutions which meet regulatory requirements and unique business process needs.
Contact: for more information on Ness Technologies’ Life Sciences solutions, please contact us at nessusasite@ness-usa.com
or call 201-488-7222 x 413. |