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Course Content
Introduction
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Clinical research Basics – Definitions, Terminology, Overview of Clinical Trials
01:13:32 -
History of Clinical Trials
29:39 -
Types of Clinical Trials & Regulatory Bodies
25:21 -
CDM Basics – Introduction
21:00 -
CDM Phases
35:47 -
CDM Phase -Setup process in-detail
01:05:19 -
CDM Phases- conduct, close out in-detail (Only Materials)
00:00
Conduct Phase: (First subject First Visit -> Last Subject Last Visit)
Close -Out Phase: (Last subject Last Visit -Data Base lock)
Set up Phase: (Protocol approval -> Go live)
Certification Exam
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About Course
Clinical Data Management
Clinical Data Management is a a vital phase of clinical research. CDM leads to high quality, reliable, and statistically sound data that ultimately reduces the time from drug development to marketing.
CDM professionals have adequate process knowledge that helps maintain the quality standards through procedures including Case Report Form (CRF) designing, CRF annotation, designing database, data entry, data validation, discrepancy management, medical coding, data extraction and database locking.
This is a uniquely tailored program for students under Unlimited Learning Program and we encourage students use the attached materials in this part of the course for preparation.
Note: We strongly instruct the students to attend the live online classes and the recordings of this program are not covered under this program.
