Good Clinical Practice (GCP) Refresher
This course is suitable for anyone involved in clinical research who has already taken a full GCP course.
Trainingonline4U Ltd
Summary
- Certificate of completion - Free
- Exam(s) / assessment(s) is included in price
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Overview
This is a professionally developed, interactive and engaging online Good Clinical Practice Refresher training course which incorporates the ICH E6 R2 update implemented in June 2017, along with the new EU Clinical Trials Regulation which became live on the 31st January 2022.
This GCP course is suitable for anyone carrying out or involved in clinical research who has already taken a full GCP course and needs a refresh in the main concepts and principles of GCP.
It was created by our subject matter expert who has worked in clinical research for over 30 years and has delivered training in GCP all around the world. The course meets the required standards for ICH GCP Investigator site personnel training, identified by Transcelerate Biopharma Inc. (this can be checked on their website).
*This is the new updated course of GCP for 2022. This most recent update ensures content remains current and includes improved knowledge checks and interaction to create a more engaging experience for our users.
You will also gain free access to our online course – “Managing Clinical Trials During COVID-19“.
Certificates
Certificate of completion
Digital certificate - Included
A certificate is downloadable immediately upon successful completion of the course. The course meets the required standards for ICH GCP Investigator site personnel training, identified by Transcelerate Biopharma Inc. (this can be checked on their website).
Resources
- Course Leaflet - download
Description
Learning Objectives
- Understand what GCP is, why it is necessary and its practical implications
- Examine key legislation surrounding GCP
- Learn the responsibilities of the key stakeholders in a Clinical Trial and how these relate to GCP
- Develop extensive knowledge and understanding of GCP to ensure compliance
- Understand the importance of key documents relating to Clinical Trials including the protocol, Investigator’s Brochure and Essential Documents
- Learn how to assess GCP compliance and understand how to effectively tackle under-performance
Who is this course for?
This GCP course is suitable for anyone carrying out or involved in clinical research who has already taken a full GCP course and needs a refresh in the main concepts and principles of GCP.
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Legal information
This course is advertised on reed.co.uk by the Course Provider, whose terms and conditions apply. Purchases are made directly from the Course Provider, and as such, content and materials are supplied by the Course Provider directly. Reed is acting as agent and not reseller in relation to this course. Reed's only responsibility is to facilitate your payment for the course. It is your responsibility to review and agree to the Course Provider's terms and conditions and satisfy yourself as to the suitability of the course you intend to purchase. Reed will not have any responsibility for the content of the course and/or associated materials.