[vc_row type=”full_width_background” bg_position=”left top” bg_repeat=”no-repeat” text_color=”dark” text_align=”left” top_padding=”70″ bottom_padding=”60″][vc_column width=”1/2″][vc_column_text]Webinar:

Integrating Clinical Trials Data for Better Research

September 3, 2015
2:00 – 2:30 PM EDT

In this webinar, you will learn how the Adaptive eClinical Bus provides you with all of the benefits cited by the FDA in their 2013 guidance on ‘‘Electronic Source Data in Clinical Investigations’’ including:

• Eliminating duplication of data by capturing and transmitting electronic source data
• Auto-populating  electronic study forms from EHRs
• Reducing transcription errors and improving the quality of data
• Encouraging entering source data at the point of care
• Facilitating remote monitoring of data to reduce the number of onsite visits
• Improving site monitoring to minimize the need for cross-reference data in multiple sources
• Making it easier for investigators to conduct clinical research
• Facilitating the inspection and reconstruction of clinical investigations by FDA

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[/vc_column][vc_column width=”1/2″][divider line_type=”No Line” custom_height=”215″][vc_column_text]Complete and submit this form to register for the “Integrating Clinical TrialsData” webinar.  After submitting the form, Adaptive Clinical Systems will email you additional information and instructions for participating in this informative session.

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