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Courses
Master Quiz to get ICH CGP Certificate
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Evolution of ICH – GCP
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Investigator Brochure
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Data Handling, Records and Data Governance
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Safety Assessment and Reporting ( Pharmacovigilance)
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Audits and Quality Assurance
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Monitoring andvRisk-Bases Quality Management (RBQM)
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Essential Documents and Trial Master File
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Protocol and Amendments ( Protocol Development)
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Sponsor Responsibilities and oversight
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Investigator Responsibilities and qualifications
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Institutional Review Board/ Independent Ethics Committee (IRB/IEC) Responsibilities
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Informed Consent
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Ethical Principles in ICH-GCP (R3)
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Clinical Research Glossary
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5.00
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Clinical Research Course Overview
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1h 15m
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