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BioClinica, Inc. to Demonstrate Technology-Enhanced Capabilities at Upcoming Global Industry Events
Date:4/3/2013

technical teams that developed each standard. The goals of these programs are to provide authoritative education in the theory and practice of using the CDISC standards, and to provide the tools and information needed to implement the standards within an organization. This training is geared toward anyone working with data in medical research including statisticians, clinical programmers, and clinical data managers. Attendees will learn how the CDISC standards can be implemented in their daily work.

  • June 4 – 5, 2013: 2-day SDTM Theory and Application
  • June 6, 2013: 1-day CDASH Implementation
  • June 7, 2013: 1-day ADaM Implementation

2nd Annual ClinTech Congress
June 11 – 12, 2013
Dublin, Ireland
The ClinTech Congress will focus on ways the pharmaceutical industry can streamline the clinical trial process through effective system management. The industry has demonstrated success leveraging clinical technology to increase effectiveness in managing clinical study information coming from a variety of sources. This conference provides in-depth knowledge on eTMF, IVR/IWR, CTMS and Portal systems, as well as building blocks for system integration. Attendees will learn how to effectively deploy an eTMF and ensure quality of documents, leverage a CTMS to streamline clinical trial processes, and examine how a portal improves oversight of study/site management. BioClinica is a sponsor of this event and will have representatives on hand to demonstrate the company's industry-leading eClinical solutions.

Jonathan Andrus , Vice President of Operations for BioClinica, will speak on the topic "Ensure Due Diligence During System and Vendor Selection."

Drug Information Association 49th Annual Meeting
June 23 – 27, 2013 
Boston, Massachusetts

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SOURCE BioClinica, Inc.
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