Integrity Clinical Compliance
provides trusted training, compliance and consultancy services to support pharmaceutical, biotech and related healthcare companies
HOLDING INTEGRITY AT THE HEART OF SCIENCE
ONLINE CLINICAL COURSES
GOOD CLINICAL PRACTICE TRAINING
POPULAR GCP TRAINING COURSES
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
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
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
WHAT PEOPLE SAY ABOUT OUR COURSES
CLINICAL CONSULTANCY SERVICES
Integrity Clinical Compliance provides experienced clinical consultancy support for life science organisations across every stage of the clinical research lifecycle. We partner with sponsors, biotechs, CROs and emerging life science businesses to deliver practical, compliant solutions that support efficient and reliable clinical operations.
Our consultancy services include clinical operations support, quality assurance, audit preparation, medical writing services and quality control review. Whether you need short-term specialist expertise, additional operational capacity or structured project oversight, our consultants bring real-world industry experience and a solutions-focused approach aligned with regulatory expectations.
RECENT BLOGS
ISO 14155:2026 Update: What’s Changed and What It Means for Clinical Investigations
The latest edition of ISO 14155, the international Good Clinical Practice standard for medical device clinical investigations, has been published....
Why Updating SOP Wording Alone Is Not Enough for ICH GCP E6(R3) Compliance
As organisations across the clinical research industry prepare for ICH GCP E6(R3), many quality and regulatory teams are asking the same question:...
What’s Changing for Clinical Trials on 28 April 2026 and What It Means for the UK and EU
The date 28 April 2026 is an important milestone for clinical trial regulation in Europe. On this day, the transition period for the EU Clinical...






