Before anyone can work on a clinical trial, they must understand ICH-GCP (Good Clinical Practice) — the globally accepted ethical and scientific standard for designing, conducting, recording, and reporting clinical research.
Whether you are a student, researcher, clinician, or healthcare professional, a strong understanding of ICH-GCP is essential for building a successful career in Clinical Research.
Speaker: Dr. Shafali Nagpal
Date: 13th June 2026 (Saturday)
Time: 7:30 PM IST
Why is ICH-GCP important?
Protects the rights, safety, and well-being of trial participants
Ensures the credibility and reliability of clinical trial data
Forms the foundation of ethical clinical research worldwide
Essential knowledge for Clinical Research, Pharmacovigilance, Regulatory Affairs, Medical Writing, and Drug Development roles
Recognized and valued by pharmaceutical, CRO, and healthcare organizations globally
Many aspiring professionals hear about ICH-GCP, but few truly understand its practical application in real-world clinical trials.
Join this exclusive training session and gain insights into:
ICH-GCP Principles
Ethics in Clinical Research
Investigator & Sponsor Responsibilities
Informed Consent Process
Essential Documents
Clinical Trial Conduct & Compliance
Real-World Industry Applications
Ideal For:
MBBS | BDS | PharmD | B.Pharm | M.Pharm | Nursing | Life Sciences Students | Researchers | Healthcare Professionals
Industry-Relevant Learning
Global Clinical Research Standards
Build a Strong Foundation in Clinical Research
The future of Clinical Research begins with understanding the standards that protect patients and ensure scientific integrity.
Register Now: