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An Institutional Review Board (IRB) or Independent Ethics Committee (IEC) plays a crucial role in e...
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Introduction to Clinical Data Management Process Overview in Pharmaceuticals, Bio-Pharmaceuticals, M...
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This document describes the detailed information of clinical trial protocol and protocol design. The...
An overview of international and Indian ethical codes for conducting research on human subjects
Informed Consent Documents are a crucial part of clinical trials. An in depth understanding of same ...
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