Inspection Readiness Fundamentals
Online Clinical Course | This course has been designed as a short demonstration of the training approach used by Integrity Clinical Compliance.
Implementing Good Clinical Practice E6(R3) Annex 2
Online Clinical Course | This course provides a practical and accessible overview of the final ICH E6(R3) Annex 2 Guideline and its considerations for modern trial designs. By the end of the course, you will understand how to apply Annex 2 requirements to your processes, technologies, and oversight responsibilities to ensure compliance across a wider range of trial settings.
ISO 14155:2026 Good Clinical Practice for Medical Devices
Online Clinical Course | Stay up to date with the latest ISO 14155:2026 standard for medical device clinical investigations. Learn what has changed, how it impacts study design, risk management, and compliance, and what your organisation needs to do to align with the new requirements.
ISO 14971:2019 Risk Management for Medical Devices
Online Clinical Course | Master ISO 14971:2019 with our practical medical device risk management training. This certified course covers hazard identification, risk analysis, control measures, and lifecycle safety, helping you meet global regulatory standards.
Conducting Clinical Trials in the UK
Online Clinical Course | This course introduces the UK clinical trial regulatory framework (effective 28 April 2026), including approvals, responsibilities, and safety oversight. It also explains how UK requirements differ from the EU system and how to manage trials involving both UK and EU sites.
Clinical Trials Regulation (EU CTR 536/2014)
Online Clinical Course | This online course covers trial authorisation, safety reporting, TMF management, and end-of-trial responsibilities, helping sponsors, investigators, and service providers run trials confidently and compliantly.
AI Application in Clinical Research
Online Clinical Course | This course covers where AI can add value, where risks arise, and how to maintain oversight, data integrity, and participant protection when AI tools are used in clinical research.
Cyber Security Awareness
Online Course | This course covers everyday topics such as protecting information, recognising scams, managing passwords, using devices securely, and knowing what to do if something goes wrong.
HIPAA for Clinical Trials
Online Clinical Course | This course explains how HIPAA protects participant information while still allowing clinical trials to be conducted effectively and compliantly.
Bridging the Gap from ICH GCP E6 R2 to R3
Online Clinical Course | This course provides a practical and accessible overview of the transition from ICH GCP E6(R2) to ICH GCP E6(R3). By the end of the course, you will understand how to adapt your processes, documentation, and oversight responsibilities to ensure compliance with the new R3 requirements.
GDPR in Clinical Trials
Online Clinical Course | Understand how GDPR applies to clinical trials with this online training course. Learn how to manage personal data lawfully, ensure compliance with EU data protection regulations, and protect participant privacy throughout the trial process. Ideal for clinical research and regulatory professionals.
Good Manufacturing Practice (GMP)
Online Clinical Course | Covering core GMP topics including quality systems, documentation, hygiene, production, warehousing, and distribution, the course also explores the role of GMP in laboratories, engineering, and trial sites; providing a functional, cross-departmental perspective.
Good Laboratory Practice (GLP)
Online Clinical Course | This professionally developed Good Laboratory Practice (GLP) training course provides a comprehensive understanding of the regulatory requirements and operational standards governing non-clinical laboratory studies.
ICH Good Clinical Practice (including E6 R3) for Investigators
Online Clinical Course | Gain essential knowledge with our ICH Good Clinical Practice (GCP) E6 R3 online training for investigators. Fully updated for 2025, this certified course meets global regulatory standards and includes 2 CPD points.
CPD Points Available: 2
Good Laboratory Practice (GLP) Refresher
Online Clinical Course | Update your knowledge with our Good Laboratory Practice (GLP) refresher course. Aligned with the latest OECD guidance, this course reinforces core GLP principles for regulatory compliance in non-clinical research.
ICH Good Clinical Practice (GCP) Refresher (Including E6 R3)
Online Clinical Course | Refresh your existing knowledge of ICH Good Clinical Practice while incorporating the latest E6 Revision 3 guidance. Ideal for those with prior GCP training, this course supports practical application in your clinical research role.
CPD Points Available: 4
Good Clinical Practice E6(R3)
Online Clinical Course | Stay compliant with global clinical trial standards through our ICH Good Clinical Practice (GCP) E6(R3) training course. Fully updated for 2026, this interactive course is suitable for all clinical research professionals and includes CPD accreditation and globally recognised certification.
CPD Points Available: 6
Informed Consent
Online Clinical Course | Gain a clear understanding of the informed consent process in clinical trials with this interactive course. Updated for ICH GCP E6(R3), this accredited training is suitable for all clinical research professionals.
PVG: Drug Safety and Regulations
Online Clinical Course | This course offers a comprehensive introduction to pharmacovigilance, providing a clear understanding of its vital role in ensuring drug safety and regulatory compliance throughout the product lifecycle.
Clinical Project Management Training
Online Clinical Course | This course will explain in everything you need to know about becoming an effective project manager within this field, from study start up right through to closeout.