ICH-Good Clinical Practice (GCP) E6 (R2) for Investigators – eLearning
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Date | Product | Location | Price | |
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ICH Good Clinical Practice for Investigators | eLearning | EUR 250 | Book | |
If you would like to have this course as an in-house session click here |
About this course
Reasons to attend
You are a principal investigator, sub-investigator, study coordinator within clinical research; or other staff; then you need to comply with the International Council of Harmonisation Good Clinical Practice (ICH-GCP) guideline, including the recently released ICH-GCP E6 (R2) Addendum 2016.Authorities as well as scientific journals imply compliance to ICH-GCP for all research with human subjects. This international standard is specifying conduct, performance, monitoring, documentation and reporting of the results of clinical research. Without training, or without experience in clinical trials, you might not fully grasp what it means to work according to GCP. This e-learning will give you the training as required by most of the European Regulators.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
- This course has been mutually recognised by TransCelerate BioPharma
- This course has been reviewed by the Belgian GCP Inspectorate.
Course schedule
- Course credit: 3h (3 months period to complete course)
- Complete the course at anytime, anywhere!
Course Description
This 3 hour course will allow professionals, active in clinical research, to understand GCP-roles of everyone involved. All GCP duties of the investigator and his/her team according to chapter 4 of ICH-GCP will be elucidated.In addition, the implementation of GCP is explained and illustrated using examples from practice. You will receive hands-on information about mandatory elements such as approval for clinical trials, informed consent, safety reporting and trial specific documentation. You will learn to link your clinical research tasks with ICH-GCP requirements.Note that the complete and most recent 2016 version of the ICH-GCP is covered by this training. Secondly, our ICH-GCP training meets all the Criteria for ICH GCP Investigator Site Personnel Training as identified by TransCelerate BioPharma, which makes this course recognized by most sponsors.Programme highlight
- Introduction to ICH-GCP for all involved stakeholders
- ICH-GCP and the 13 responsibilities of the investigator and his /her staff
- Being qualified, taking responsibility and having oversight
- Obtaining informed consent, the right way
- Knowing and following the protocol
- Controlling the investigational products
- Safety reporting characteristics
- Source documents and trial specific documents
Learning objectives
- Comprehend the overall ICH-GCP requirements
- Understand the responsibilities of a Medical Doctor within clinical trials
- Know what, why and how clinical trial duties are to be performed and documented
- Be prepared for audits/inspections
Who should attend
Medical Doctors looking to participate in, or conducting Clinical Trials. Sub-investigators, study coordinators and other staff involved in clinical trials.
Competencies
This course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design (0)
- Ethical & Participants Safety Considerations (2)
- Investigational Product Development and Regulation (4)
- Clinical Studies Operations (GCPs or ISO 14155) (8)
- Study and Site Management (2)
- Data Management and Informatics (4)
- Leadership and Professionalism (2)
- Communication (0)
- Teamwork (0)
- Business acumen (0)
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