Expediting Clinical Site Initiation and Streamlining Site Monitoring with Digital Signatures
Thursday, December 2, 2010 at 2:00pm EST
» Register Free Here
Event Overview:
Learn how digital signatures enhance clinical operations – from expediting site initiation to completing site monitoring and streamlining quality, audit and compliance. Save time and money by replacing paper and routing with compliant digital signatures.
Live case studies will be presented about use of digital signatures in clinical operations by top 10 Biopharmas, CROs and software/service vendors offering document and quality management systems, investigator portals, and clinical trial management systems.
Key Learning Objectives:
- How to initiate clinical sites more quickly and cost-effectively by enabling investigators and IRBs to digitally sign regulatory packet documents and forms.
- How to expedite and minimize the costs of site monitoring reporting by CRAs.
- How to ensure document security and compliance to efficiently support FDA audits with digitally signed documentation.
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Clinical Operations |
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Clinical Informatics |
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QA, RA, and Clinical IT Professionals from CROs |
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Study Sponsors |
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Clinical Technology Vendors |
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| Moderator |
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Jeff Schindler
Managing Editor
Pharmaceutical Executive |
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| Presented By |
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Rodd Schlerf
FDA and USDA Markets Manager
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