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Phases 1, 2, 3 and 4 |
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Contract and Budget
Negotiations |
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Submission for
Institutional Review Board or Independent Ethics Committee (IRB/IEC)
Approval |
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Patient Recruitment |
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Patient Follow-up |
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Site Initiation and Trial Close-out Operations |
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Trial-related Documents Archival and Maintenance |
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Precise and Accurate Data Entry |
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Ensuring Protocol Compliance |