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ICH-GCP : Good Clinical Practice

Comprehensive Modules for In Depth Knowledge (Read Only)

Created byProRelix Education

Last updated 3/2020

English

What you'll learn

ICH GCP E6(R2)

Course content

1 section • 8 lectures • 1h 32m total length

Introduction to Training Modules0:17
Module 1: Introduction, Background & History of ICH GCP8:43
Module 2: Glossary19:35
Module 3 : Principles of ICH GCP6:05
Module 4 : Roles & Responsibilities of IRB/IEC11:10
Module 5 : Roles & Responsibilities of Sponsor21:48
Module 6 : Roles & Responsibility of Investigator14:33
Module 7 : Essential Documents10:15

Requirements

Pharmacy or Lifesciences background

Description

This course gives an opportunity to get in depth knowledge of ICH GCP.

Who Should Enroll?

Any Life Science/ Pharmacy/ Nursing/ Medical/ Dental Graduate or Post Graduate
Industry People: Clinical Research Coordinator, Clinical Research Associate, Clinical Data Coordinator, Drug Regulatory Affairs Executive, Ethics Committee Members, Clinical Site Personnel, Any Professional Involved directly or indirectly in Clinical Research Activities

What This Course Covers?

Module 1 Introduction purpose history of ICH GCP
Module 2 Glossary Core Principles
Module 3 13 core principles
Module 4 Roles and responsibilities – IEC
Module 5 Roles and responsibilities - Sponsor
Module 6 Roles and responsibilities – Investigator
Module 7 Essential documents

What Benefits/ Value This Course Offer?

Upgrade Yourself With New ICH GCP E6R2 Update
Content Developed By Industry People With 15+ Years of Experience
Self Paced Learning

Who this course is for:

Clinical Research Organizations staff, students