Direct Data Extraction and Exchange of Local Labs for Clinical Research Protocols:
A Partnership with Sites, Biopharmaceutical Firms, and Clinical Research
Organizations
Date: June 16
Time: 08:00 AM PDT | 11:00 AM EST | 17:00 CET | 21:30 IST
Manual transcription of site clinical trial data into sponsor Electronic Data
Capture (EDC) systems is labor intensive and error prone. During this webinar, we
will describe
Direct Data Extraction (DDE) best practices identified by the
Society for Clinical Data Management eSource Consortium that will
enable other
groups to implement DDE for their own clinical research efforts
.
The primary objective of this webinar is to discuss the efficiency gains and
return on investment for implementing DDE compared to traditional manual data
entry methods
. We'll discuss our experience and learnings from our proof of
concept with two biopharmaceutical companies and another academic medical center.
We'll present the return on investment for DDE versus manual data entry via the
following productivity surrogate markers: data latency, queries, transcription
errors, and monitoring activity.
WHAT YOU'LL LEARN
- Direct data extraction best practices for sites, biopharmaceutical firms, and CROs interested in implementing DDE;
- How DDE is still highly valuable versus HL7-FHIR methods of transfer;
- How to get DDE off the ground with your site or firm;
- How is DDE received by site staff, biopharmaceutical firms, and CROs.
WHO SHOULD ATTEND
This webinar is targeted at beginners wanting to learn more about DDE. It also applies to intermediate and advanced audiences with respoect to how DDE compares to HL7-FHIR and other eSource modalities.
ABOUT THE SPEAKER
 |
Michael Buckley, MS, MBA Enterprise Innovation Manager, Clinical Research Informatics and Technology Enterprise, Clinical Research Administration |
Michael is also Past Co-Chair of SCDM's eSource Implementation Consortium.