Скачать или смотреть Responsibilities of the IRB/IEC in Clinical Trials | Ethics, Oversight, and Compliance Explained

Responsibilities of the IRB/IEC in Clinical Trials | Ethics, Oversight, and Compliance Explained

Responsibilities of the IRB/IEC in Clinical TrialsIRB responsibilitiesIEC in clinical trialsClinical trial ethicsHuman subject protectionGCP complianceInstitutional Review BoardIndependent Ethics CommitteeMedical Affairs trainingClinical research governanceProtocol review process

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Описание к видео Responsibilities of the IRB/IEC in Clinical Trials | Ethics, Oversight, and Compliance Explained

What Responsibilities of the IRB/IEC in Clinical Trials ?
Institutional Review Board (IRB) or Independent Ethics Committee (IEC)

In this tutorial, you’ll discover the critical responsibilities of IRBs/IECs—from safeguarding human subjects to reviewing protocols and monitoring ongoing ethical compliance.

We’ll break it down into 3 key sections:

🔹 Structure and Function of IRBs/IECs – How they’re formed and what they are accountable for
🔹 Relationship with Investigators – Oversight, communication, and continuing review
🔹 Relationship with Sponsors – Submissions, ethical obligations, and transparency

This tutorial is essential for investigators, Medical Affairs professionals, and clinical research teams who need to understand the ethical foundation of every clinical study.

📅 Stay compliant. Stay informed.
🎯 Start mastering IRB/IEC requirements today.

#IRB #IEC #ClinicalTrials #EthicsInResearch #ClinicalResearchTraining #MedicalAffairs #GCP #HumanSubjectProtection #IRBResponsibilities #SkyHealthAcademy

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