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The top documents tagged [irb approval letter]
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irb approval letter
Maximum 3 pages 12-point type Double spaced List item by item in order listed in Budget Section C If have the space, note company names for.
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Regulatory Submission Process Clinical Study Application: 1. Submit an appointment requestappointment request 2. Fill one of the three templates: - BE.
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Laura Noll Research Compliance Manager Radford University.
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The Right Prescription for Working with Investigational Drug Service at BMC Andrew Schoch Pharmacy Intern Northeastern University Class of 2010 Hyeseon.
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Research and Development Protocol Submission and Continuing Review Processes Kimberly Summers, PharmD Assistant Chief for Clinical Research South Texas.
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Renewals A HOW-TO. Objectives 1.Why are renewals necessary? 2.What projects require a renewal? 3.How do I find the form? 4.How do I fill out the form?
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NCI Clinical Trials Reporting Program CTRP User Meeting February 9, 2011.
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Business Operations Pre-Award. What is required to begin the business process? Possible indicators CDA executed Cancer Center MDG/PRC approvals Department.
212 views
The Right Prescription for Working with Investigational Drug Service at BMC
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