Good Clinical Practice (ICH GCP) for Clinical Research

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(5 Ratings)

Offered byUDEMY

Good Clinical Practice (ICH GCP) for Clinical Research
at
UDEMY
Overview

An Introduction to Good Clinical Practice ICH GCP E6 (R2) for Investigators & Clinical Research Staff

Duration	2 hours
Total fee	₹1,999
Mode of learning	Online
Credential	Certificate

Good Clinical Practice (ICH GCP) for Clinical Research
at
UDEMY
Highlights

Earn a certificate of completion from Udemy
Learn from 1 downloadable resources & 2 articles
Get full lifetime access of the course material
Comes with 30 days money back guarantee

Good Clinical Practice (ICH GCP) for Clinical Research
at
UDEMY
Course details

Skills you will learn

Compliance

Who should do this course?

For Anyone who wants to elevate their GCP knowledge

What are the course deliverables?

Comprehend the key ICH-GCP requirements and regulatory expectations regarding conduct of clinical trials
Understand the responsibilities of an investigator/ investigator team within clinical trials
Know what, why and how clinical trial activities are to be performed and documented
Learn about the quality issues affecting clinical research

More about this course

This training course will help professionals, whether currently active in clinical research or planning to be involved, to understand their GCP roles and to manage a GCP compliance clinical trial
The learners will receive information regarding key elements such as informed consent, investigational products handling, safety reporting and trial specific documentation, including data integrity key principles

Good Clinical Practice (ICH GCP) for Clinical Research
at
UDEMY
Curriculum

Introduction

ICH Good Clinical Practice (GCP) Course Overview

ICH GCP Overview

ICH GCP Overview

The Principles of ICH GCP

The Principles of ICH GCP

Investigator's Responsibilities

Investigator's Qualifications & Agreements (ICH GCP 4.1)

Adequate Resources

Adequate Resources (ICH GCP 4.2)

Medical Care of Trial Subjects

Medical Care of Trial Subjects (ICH GCP 4.3)

Good Clinical Practice (ICH GCP) for Clinical Research
at
UDEMY
Faculty details

Dr. Leire Zuniga

Dr Leire Zuniga is the Founding Director and Principal GCP Consultant of Pharmity. Pharmity is a consultancy firm with headquarters in Spain that delivers quality consultancy, auditing and online training services globally to the pharmaceutical and biotechnology industry.