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Reflections From The ICR Conference 2026
We recently had the opportunity to attend the ICR Conference in Birmingham, hosted by the Institute of Clinical Research. It’s always valuable...
ISO 14155:2026 Update: What’s Changed and What It Means for Clinical Investigations
The latest edition of ISO 14155 2026, the international Good Clinical Practice standard for medical device clinical investigations, has been...
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...
Common GCP E6(R3) Misunderstandings and How to Avoid Inspection Findings
The implementation of ICH Good Clinical Practice E6(R3) marks one of the most significant shifts in clinical trial governance in decades. Yet many...
Why Cyber Security Matters More Than Ever
Cyber security is no longer just an IT issue. It affects anyone who uses email, shops online, works remotely, or stores information digitally. From...
Understanding the New UK‑Specific Annotations to ICH GCP E6(R3)
The UK clinical research landscape continues to evolve, and this week the Medicines and Healthcare products Regulatory Agency (MHRA) published...
Welcome to Our New Brand: Integrity Clinical Compliance
We’re delighted to share an exciting update about the next chapter in our business journey. As many know, over the years, our work has grown far...
Why Training Is Essential for the New ICH GCP Annex 2 – And How We’re Getting You Ready
The clinical research landscape is changing once again with the introduction of ICH GCP Annex 2 a long-awaited extension expected to be finalised...