Good Clinical Practice (ICH GCP) for Clinical Research

Good Clinical Practice (ICH GCP) for Clinical Research

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...

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

Url: View Details

What you will learn

• 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
• 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

Rating: 3.81481

Level: All Levels

Duration: 1.5 hours

Instructor: Dr. Leire Zuñiga