As one of few vendors responding to the FDA call for greater use electronic data capture and integration, Adaptive Clinical Systems was pleased to be invited by CDISC to participate in a “eSource Stakeholders Group” with the FDA and two dozen other vendors – contributing to the discussion and insight from drawn from experience on the subject.
The Working Group session will take place in Washington, DC on March 18th, 2016. This collaborative exchange of ideas and experiences is hosted by The Clinical Data Interchange Standards Consortium (CDISC). CDISC is a global, open, multidisciplinary, non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. The CDISC mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare. CDISC standards are vendor-neutral, platform-independent and freely available via the CDISC website.
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