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CareLex Builds Support for Developing Interoperability Standard for Clinical Trial Data Exchange
Date:9/4/2013

ene an eTMF Technical Committee at OASIS in the coming weeks.

"At OASIS, we are committed to coordinating our efforts with BioPharma stakeholders and regulatory agencies worldwide to advance the development of specifications that leverage interoperable standards for the clinical trials area," said Laurent Liscia, executive director and CEO of OASIS. "We look forward to advancing the eTMF work."

Individuals with demonstrated expertise in domain areas related to clinical trial content classification, regulatory compliance, content management or software information modeling are invited to take a leadership role in the eTMF standardization initiative. Participation will be open to all interested parties. Details are available by contacting Zack Schmidt via the CareLex website at http://www.CareLex.org or email at admin(at)CareLex(dot)org, OASIS, or email at join(at)oasis-open(dot)org. Join the new LinkedIn eTMF Standards discussion group at http://www.linkedin.com/groups/eTMF-Standards-5161997/about.

About CareLex

CareLex™ is a non-profit public benefit organization for BioInformatics research and development. Organized in 2012 by a core group of clinical trial domain and bioinformatics experts, CareLex provides open source technology for BioPharma content classification and management. CareLex is open to anyone worldwide. For more information, visit http://www.CareLex.org/.

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