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 can be used to speed up clinical site initiation, cut costs in site monitoring reporting, enhance and eClinical portal/CTMS, and streamline regulatory compliance and audits (with or without a document management system).
Live case studies will be presented on the 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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