Good Clinical Practice (Gcp) In Clinical Research

What you'll learn
Introduction to Good Clinical Practices (GCP)
History of ICH-GCP Guidelines
13 Principle of Good Clinical Practices
Major Stakeholders in Clinical Trials
ICH E6 Efficacy guidelines for Clinical Trials
ICH-GCP E6 R(3) Amendment
Understanding important updates in E6 R(3) Amendment
Risk-Based Approach to Clinical Trials
Data Quality and Integrity in Clinical Trials
Informed Consent in Clinical Trials
Quality Management System (QMS)
Quality by Design (QbD) in Clinical Trials
Patient Centric Clinical Trials
Understanding Sponsor role & responsibilities
Understanding Ethics Committee role & responsibilities
Understanding Principle Investigator role & responsibilities
Understanding Study participants role & responsibilities
Understanding Regulatory Authority role & responsibilities
Monitoring Clinical Trial process
Risk Based Monitoring
Ethics in Medical Research
Ethical conduct of Clinical Trials
Informed Consent in Clinical Trials
Protocol compliance in Clinical Trials
Ethics Committee/ IRB in Clinical Trials
Clinical Trial Data Management
Requirements
No prerequisite is needed for this course.
Description
Master the Global Standard That Governs Clinical Trials Worldwide!Good Clinical Practice (GCP) is the foundation of ethical, high-quality, and compliant clinical research.If you are a Pharmacy, Life Sciences, Biotechnology, or Medical graduate looking to build a career in Clinical Research, CROs, Pharma Companies, or Hospitals, this course is designed exactly for you.This comprehensive GCP Masterclass takes you from basic concepts to real-world application, explained in simple, easy-to-understand language, with practical examples and industry-relevant insights.Why Choose This Course?Many students memorize GCP guidelines but struggle to apply them in real clinical trials.This course bridges that gap by explaining not just WHAT GCP says, but HOW it is implemented at sites, by sponsors, and during monitoring.Whether you are:A student preparing for interviewsA working professional upskilling for career growthSomeone transitioning into clinical research or pharmacovigilanceThis course will give you clarity, confidence, and job-ready knowledge.What You Will LearnBy the end of this course, you will be able to:Understand the principles and importance of Good Clinical PracticeExplain ICH-GCP E6 (R2/R3) guidelines with confidenceUnderstand ethics in clinical research and patient protectionUnderstand roles & responsibilities of Investigator, Sponsor, Regulatory Authority, CRO, and Study participantsGain clarity on concepts like Risk-based approach, Quality by Design, Informed Consent, Quality management systemsUnderstand monitoring, auditing, and regulatory inspectionsUnderstand essential Guidelines, Updates and Latest amendmentsPrepare confidently for Clinical Research interviewsHow This Course Is Structured Step-by-step learning from beginner to advanced Simplified explanations of complex guidelines Real-world examples and case-based learningIndustry-focused approach aligned with CRO & Pharma expectationsDesigned for students with no prior clinical research experienceGood Clinical Practice is not optional - it's essentially the License to Work in Clinical Research.Enroll now and build a strong foundation for a successful career in Clinical Research, Pharma, and Life Sciences.Click ENROLL NOW and take your first step toward a compliant and confident CLINICAL RESEARCH CAREER!
Students & Professionals exploring Career opportunities in Clinical Research,Pharmacy graduates curious about Drug development & Clinical Trials,Pharmacy, Biotechnology, Lifesciences, Chemistry & Medicine graduates,Anyone curious about understanding Ethical trials conduct & Regulatory requirements,Professionals from Clinical Research, Clinical Data Management & Pharmacovigilance,Quality and Regulatory Affairs Professionals in Clinical Trials
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