(60 minutes) Sponsors use many external vendors including CROs and multiple clinical sites during clinical trials. Based on the technical fluency of the users at these sites the documents and content that sponsors receive back may not be as usable as they could be. How do we put concepts in place that enable us to have a more consistent level of quality in documents?
This webinar informs content structure details that are often misunderstood and have significant impact on interoperability:
– Scanned images and the difference between Image files and OCRed content
– Standard formatting for ease of consolidation
– Content mapping to generate summary data
PANELISTS
Mark Gross, President, Data Conversion Laboratory
Keith Parent, CEO, Court Square Group
Ron Niland, President, JANA Life Sciences
This webinar is the fifth in a series to inform Life Science organizations about technology considerations related to the creation and management of content and technical data.
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