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ICH Good Clinical Practice (including E6 R3) for Investigators

GOOD CLINICAL PRACTICE E6(R3) FOR INVESTIGATORS TRAINING COURSE INFORMATION

GCP for Investigators Online Course
£99
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Build a practical understanding of your responsibilities as a clinical trial investigator under ICH Good Clinical Practice E6(R3).

Developed by experienced clinical research professionals, this online GCP course focuses on the requirements relevant to investigators and research-site personnel, including participant protection, informed consent, trial oversight and reliable records.

The self-paced training is suitable for individual learners and organisations providing consistent GCP training across their investigator teams.

Current Status

Not Enrolled

Price

£99.00

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KEY FEATURES OF OUR ONLINE GCP FOR INVESTIGATORS TRAINING COURSE:

  • Fully online and available on demand
  • Complete your learning at your own pace
  • Focused on investigator and research-site responsibilities
  • Covers ICH GCP E6(R3) principles and requirements
  • Developed by experts with more than 35 years of clinical research experience
  • Interactive content, practical examples and knowledge checks
  • Certificate awarded following successful completion
  • Approved by the Faculty of Pharmaceutical Medicine for 2 CPD points
  • Individual enrolment and team licences available

The Faculty of Pharmaceutical Medicine has approved this online GCP for Investigators training course for CPD points.

CPD POINTS AVAILABLE: 2

Course Content

GCP (including E6 R3) for Investigators

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PRACTICAL GCP TRAINING FOCUSED ON INVESTIGATOR RESPONSIBILITIES

Investigators play a central role in protecting clinical trial participants and ensuring that research is conducted appropriately at their site. Understanding how Good Clinical Practice applies to these responsibilities helps support sound decisions, effective oversight and reliable trial results.

Our online ICH GCP E6(R3) for investigators course combines foundational GCP knowledge with the changes introduced in Revision 3, focusing on their implications for investigators and site teams.

You will explore participant safety, informed consent, risk-based approaches, monitoring and site management. The course also examines data integrity, the use of technology and the essential records needed to document trial activities.

Practical explanations and interactive knowledge checks help you connect GCP requirements with the situations you may encounter in clinical research. The aim is to strengthen your understanding of both your own responsibilities and how your work contributes to the quality of the wider trial.

GCP TRAINING FOR INDIVIDUAL INVESTIGATORS AND RESEARCH TEAMS

INDIVIDUAL LEARNERS

Training for individuals

Develop your understanding of ICH GCP E6(R3) for investigators at a time and pace that fits around your clinical and research commitments. Complete the course to receive your training certificate and gain 2 CPD points.

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CORPORATE TEAMS

Corporate training

Provide consistent training for investigators and research-site colleagues across your organisation. Our team licences support multiple learner enrolment, progress tracking and centralised training administration.

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WHAT WILL I LEARN FROM THIS GCP TRAINING FOR INVESTIGATORS?

This course explains the GCP principles and requirements relevant to investigators, with a focus on applying ICH E6(R3) in clinical trial practice.

Identify the key changes introduced by ICH GCP E6(R3) and their impact on investigator and site responsibilities.

Apply the core principles of GCP to support ethical, compliant and high-quality clinical trial conduct.

Apply risk-based approaches to participant safety, trial oversight, monitoring and site management.

Apply GCP requirements for informed consent, data integrity, technology and essential records in your role as an investigator or site professional.

FREQUENTLY ASKED QUESTIONS ABOUT GCP TRAINING FOR INVESTIGATORS

What is GCP training for investigators?

Good Clinical Practice training helps investigators understand the ethical and scientific principles that underpin clinical trials and the responsibilities associated with conducting research at a trial site.

This course focuses on ICH GCP E6(R3), including participant protection, informed consent, oversight, data integrity and essential records. It connects these requirements with the work of investigators and research-site personnel.

Does this course cover ICH GCP E6(R3)?

Yes. The course covers ICH GCP E6(R3) alongside foundational GCP principles.

It explores the changes introduced in Revision 3 and their relevance to investigator responsibilities, including risk-based approaches, participant safety, monitoring, technology and data quality.

Can I complete the investigator GCP course online?

Yes. The course is fully online and self-paced, allowing you to fit your training around clinical duties, research activities and other commitments.

There are no fixed classroom sessions, making it suitable for individual professionals and teams working across different sites.

Can organisations purchase multiple course licences?

Yes. We offer team licences for organisations training multiple investigators or research-site colleagues.

Corporate options support learner enrolment, progress monitoring and centralised training management. Contact us with your team size and requirements to receive a tailored quotation.

Will I receive a GCP certificate?

Yes. You will receive a certificate after successfully completing the course, providing evidence of your ICH GCP E6(R3) training.

If you need the course to meet a particular sponsor’s or institution’s training requirements, check those requirements before enrolling.

Does this course provide CPD points?

Yes. The Faculty of Pharmaceutical Medicine has approved this online GCP training course for investigators for 2 CPD points.

If you need the course to meet a particular sponsor’s or institution’s training requirements, check those requirements before enrolling.

What makes Integrity Clinical Compliance’s training different?

Our training is developed by experienced clinical research professionals and focuses on how GCP requirements apply to investigator and site responsibilities.

Practical examples, interactive content and knowledge checks help you understand the reasoning behind the requirements and relate them to your work. The course addresses both foundational knowledge and the implications of ICH GCP E6(R3).

Who should complete this GCP course?

This course is designed for investigators and research-site personnel involved in clinical trials, including:

  • Principal investigators
  • Sub-investigators
  • Research physicians
  • Research nurses
  • Study coordinators
  • Site managers and other research-site personnel

It is suitable for professionals developing their initial GCP knowledge and those seeking to refresh their understanding of investigator responsibilities under ICH GCP E6(R3).

How does this differ from the full GCP course or GCP refresher?

This course focuses specifically on investigator and research-site responsibilities.

Our Good Clinical Practice E6(R3) course provides broader training for clinical research professionals, while our GCP Refresher E6(R3) course is intended for learners updating existing GCP knowledge.

Choose the course that matches your role, previous training and the requirements of your organisation or trial sponsor.

If this course isn’t right for you, take a look at our other online clinical courses.