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SOLTI Central Office offers an exceptional support in the following areas:
• Protocol writing
• CRF and IC design
• Regulatory and administrative activities during clinical trial setup
• Assessment to investigator’s team
• Investigator’s team resources
• Data management and statistics
• Trial audits preparation
• Manuscript writing and submission to journal editor
• Personnel training in clinical research
• Regulatory updates
• Scientific events sponsorship
• Community building activities
• Facilitation of communication among members
• Facilitation of communication with the sponsor
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