Good Clinical Practice (ICH GCP) for Clinical Research
- 4.1
Brief Introduction
An Introduction to Good Clinical Practice ICH GCP E6 (R2) for Investigators & Clinical Research StaffDescription
CONDUCT A SUCCESSFUL CLINICAL TRIAL JUST GOT EASIER…You’re Just Seconds Away From The Essential Good Clinical Practice (GCP) Training & Advice!
“ICH Good Clinical Practice (GCP) E6 (R2) for Investigators and Clinical Research staff”
INTRODUCING THE GOOD CLINICAL PRACTICE GCP COURSE
A course designed not only for investigators and site staff but also its content is key for CRAs, Clinical Operations staff, Clinical QA, and Regulatory Affairs departments.
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.
THIS INTRODUCTORY GCP COURSE WILL HELP YOU TO:
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
Enroll today (30 day money back guarantee) to be inspection ready...
Requirements
- Requirements
- It doesn’t matter if you are completely new to GCP and no prior GCP knowledge is necessary to participate in this course