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Building a reliable, scalable, secure applications could happen either following verified design pat...
Clinical trials are divided in to different phases –Phase 1, Phase 2 and Phase 3 each of which has...
The Investigator's Brochure (IB) is a document that serves as a comprehensive reference manual f...
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Blinding is a procedure in which one or more parties in a trial are kept unaware of which treatment...
Clinical Data Management (CDM) is a critical component of clinical research that involves the collec...
A document outlining trial objectives, design, methodology, and analysis plan.��It serves as a r...
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Regulatory aspects of clinical trials refer to the rules, regulations, and guidelines set forth by r...
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A clinical protocol defines the plan for a clinical trial, detailing every aspect of how the study w...
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Clinical trials are fundamental to the development and approval of new drugs, ensuring their safety,...
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clinical trial designs
This presentation gives an overview on Clinical trial Protocol development
