ICH GCP E6 (R3) Supplementary Training
(Valid ICH GCP (R2) training certificate required)
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eLearning course
Course type
2 hrs
Study time
Online
Mode of learning
2 CPD points
1 Clinical, 1 Ethics
(80% average required)
(80% average required)
Course overview
This course is for all clinical research professionals and stakeholders
(CRO’s, Biopharmaceuticals, Sponsors, Clinical Research Sites & Ethics Committees) around the globe who have a current valid ICH GCP E6 (R2) certification.
(CRO’s, Biopharmaceuticals, Sponsors, Clinical Research Sites & Ethics Committees) around the globe who have a current valid ICH GCP E6 (R2) certification.
The review of the ICH GCP E6 (R3) guidelines has reached Step 4, with the final version adopted on 06 January 2025, which means the guideline is now considered complete and is endorsed by the ICH Assembly.
This also means that the member regulatory authorities of ICH (such as the FDA, EMA, PMDA, etc.) have formally adopted the guideline into their respective regulatory frameworks, which means the guideline is now part of the official regulatory requirements in these regions, and should be followed by all stakeholders and individuals conducting clinical trials or working in drug development.
The course has been designed by industry experts to ensure you stay up to date with the latest regulations to conduct high quality clinical trials. The ICH GCP E6 (R3) course is designed to help you digest the extensive updates made, by taking you through each section step-by-step. See below for more information on the course.
Enrol now to stay compliant!
Who is this course for?
Individuals with a current valid ICH GCP E6 (R2) certificate working in the industry.
As such, this course is perfect for Clinical trial assistants (CTAs), Clinical research nurses (CRNs), Clinical Study Coordinators, Investigators, Research Pharmacists, CRA’s, Central Monitors, Data capturers, Data Managers, Statisticians, Project Managers, Regulatory Specialists, Quality Assurance staff, Internal monitors, Clinical Laboratory Staff, Recruiters, Members of a community advisory board (CAB), Pharmacovigilance staff, Ethics committee members, Auditors, GCP training providers etc.
As such, this course is perfect for Clinical trial assistants (CTAs), Clinical research nurses (CRNs), Clinical Study Coordinators, Investigators, Research Pharmacists, CRA’s, Central Monitors, Data capturers, Data Managers, Statisticians, Project Managers, Regulatory Specialists, Quality Assurance staff, Internal monitors, Clinical Laboratory Staff, Recruiters, Members of a community advisory board (CAB), Pharmacovigilance staff, Ethics committee members, Auditors, GCP training providers etc.
Required qualification
This is a supplementary course, and does not confer GCP compliance alone.
This course ONLY provides training to current GCP certified professionals on the updates made from ICH GCP E6 (R2) to (R3).
This course ONLY provides training to current GCP certified professionals on the updates made from ICH GCP E6 (R2) to (R3).
As such, you must be in the possession of a current valid ICH GCP (R2) training certificate, to take this course.
If you need GCP compliance, you can enrol on our FULL GCP course here.
If you need GCP compliance, you can enrol on our FULL GCP course here.
Develop Your Professional Skills
Why choose TASK Research Academy?
Among Clinical Research Academies, TASK Research Academy stands out as uniquely positioned to comprehend challenges, forge new narratives, and lead positive transformation, not only within Africa, but worldwide.
It's not only what we teach, but how we teach that sets us apart. At TASK Research Academy, we specialise in creating immersive, simulation-based learning that breaks down silos in the industry, by situating content within the context of the entire clinical trial lifecycle.
In addition, our courses are narrative-driven, have a logical flow, are easy to understand, and are full of practical tips and tools developed to help the individual with the day-to-day experiences of working in clinical trials.
In addition, our courses are narrative-driven, have a logical flow, are easy to understand, and are full of practical tips and tools developed to help the individual with the day-to-day experiences of working in clinical trials.
Our mission presents an exceptional opportunity to shape a new global perspective on compliance and competency training, assisting in professionalising the clinical research industry.
Our goal is to be an international one-stop shop for all your clinical trial training needs, by providing a solution for individuals from being research-naïve to hitting the ground running.
Our goal is to be an international one-stop shop for all your clinical trial training needs, by providing a solution for individuals from being research-naïve to hitting the ground running.
About TASK Research Academy
At TASK Research Academy, we believe that learning should be fun, interactive, and immersive. That’s why our programmes are crafted by industry experts to ensure they meet the highest standards and best practices. We are dedicated to providing training that is not only high-quality and comprehensive but also flexible and accessible, catering to the needs of individuals and businesses alike.
Join us on a journey to unlock your potential and achieve professional certification through our courses. Whether you’re a newcomer looking to break into the field or a seasoned professional seeking to enhance your skills, Task Research Academy is your ultimate destination for career development in clinical research.
Step into the future of clinical research training with us and watch your career soar!
Quality Assured
Established in 2022
Trusted Provider
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