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CDISC is “a global, open, multidisciplinary, non-profit organisation that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata”. Through Gold Membership, CROS NT will have the following benefits:
• Access to new documentation for CDISC standards
• CDISC Case Studies and Business Cases
• Tools and presentations
• Access to new data standards and useful information
CDISC also provides public training courses and webinars as well as virtual learning opportunities.
In the field of Clinical Data Management, CROS NT prides itself on its thorough understanding of industry trends and regulatory standards. In order to manage vast amounts of clinical trial data in an efficient and cost effective manner, CROS NT relies on the CDISC data standards.
“As CDISC is a world-wide industry recognized standard and requested for FDA submissions, CROS has developed the knowledge and expertise to meet the CDISC requirements and at the same time satisfy Sponsors requirements by harmonizing reporting standards across studies and increasing efficiency and quality in the deliverables to Sposors”, says Monica Pimazzoni, Head of Clinical Data Management for CROS NT.
The CROS NT Member Profile can be found on the CDISC website:
http://www.cdisc.org/
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CROS NT Group, an international Contract Research Organisation (CRO), with headquarters in Verona, Italy, has built a strong heritage in biostatistics as well as providing clinical data management, medical communication, pharmacovigilance, and technology solutions to the life science industry. Founded in 1992, CROS NT is well-established in delivering quality, timely, and cost effective service.
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