About Course
Start your journey in Clinical Research with industry-focused training designed to build strong fundamentals and practical skills. Learn ICH-GCP E6 (R3), regulatory guidelines, study start-up, protocol compliance, ALCOA+, and much more through a self-paced online program. Whether you’re a Life Science graduate, healthcare professional, or an aspiring Clinical Research professional, this course can help you take the next step in your career.
Course Content
How to Access Learning Modules
🎓 How to Access Learning Modules and Sessions | Quick Step-by-Step Guide
Welcome! In this tutorial, you’ll learn exactly how to access and navigate your learning modules and training sessions with ease. Whether you're accessing video lessons, downloadable materials, or live classes, this video will walk you through the entire process.
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Quick Step-by-Step Guide
Module 1
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1.1 Life Sciences Industry Overview
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Assessment Form 1.1
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1.2 Indian Life Sciences Industry Overview
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Assessment Form 1.2
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1.3 Global Life Sciences Industry Overview
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Assessment Form 1.3
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1.4 Introduction to Clinical Research
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Assessment Form 1.4
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1.5 Stakeholders
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Assessment Form 1.5
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1.6 Regulatory Framework in India
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Assessment Form 1.6
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1.7 Global Regulations and Guidelines-2
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Assessment Form 1.7
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1.8 Ethics in Clinical Research
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Assessment Form 1.8
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1.9 Good Clinical Practice (GCP) Guidelines
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Assessment Form 1.9
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1.10 Documentation in Clinical Trials
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Assessment Form 1.10
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1.11 Safety Reporting In Clinical Trials
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Assessment Form 1.11
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1.12 Skills Required in Clinical Research
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Assessment Form 1.12
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1.13 Job Roles Clinical Research
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Assessment Form 1.13
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1.14 Importance of Skilled Professionals in Clinical Research Ver2.0
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Assessment Form 1.14
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1.15 Clinical Research Career Pathways and Professional Readiness
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Assessment Form 1.15
Module 2
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2.1 Introduction to Clinical Trial Management
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Assessment 1
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2.2 Clinical Trial Lifecycle
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Assessment 2
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2.3 Clinical Trial Phases and Regulatory Requirements
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Assessment 3
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2.4 Clinical Study Protocol Development
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Assessment 2.4
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2.5 Informed Consent Document (ICD)
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Assessment 2.5
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2.6 Clinical Trial Site Feasibility & Site Selection
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Assessment 2.6
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2.7 Introduction to Budgeting & Financial Management
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Assessment 2.7
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2.8 Resource Allocation & Trial Planning
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Assessment 2.8
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2.9 Clinical Trial Data Collection & Management
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Assessment 2.9
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2.10 Clinical Trial Monitoring & Audit
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Assessment 2.10
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2.11 Protocol Deviations and CAPA Management
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Assessment 2.11
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2.12 Ethics and Patient Confidentiality
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Assessment 2.12
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