Regulatory Updates, GCP Training Courses & QP Excellence Top Tips
In this EPiC Update, we start the year by focusing on what matters most: robust GXP compliance, clear regulatory understanding, and practical support for the professionals driving quality across the pharmaceutical and clinical research landscape.
This edition highlights recent UK regulatory guidance, including updates to the MHRA Clinical Trials Hub and the practical implications of ICH E6(R3) for organisations running clinical trials in the UK. We also spotlight EPiC’s GCP training pathway – from introductory content for those new to clinical research through to a full‑day foundations course for those ready to deepen their expertise and prepare for inspections.
For Qualified Persons (QPs), we share actionable leadership and compliance To Tip from EPiC’s Operations Manager, Michelle Yeomans, designed to support both trainee and experienced QPs in navigating evolving expectations.
In this edition, you’ll find:
- UK regulatory updates focusing on MHRA Clinical Trials Hub changes and ICH E6(R3) in a UK context
- An Introduction to Good Clinical Practice (GCP) for those starting out in clinical research
- GCP Foundations for Compliance, a full‑day course exploring the practical application of GCP in trial conduct and inspections
- Top Tips for Qualified Persons (QPs) to support leadership, GMP compliance, and ongoing professional growth
- A Meet the Team spotlight on Company Administrator Michelle Harkness
Whether you are building foundational knowledge or enhancing established expertise, this edition is designed to help you stay ahead in the regulatory landscape.
WHAT DO YOU REQUIRE?
WE SPECIALISE in helping pharmaceutical and biotechnology companies, as well as other associated healthcare clients, to achieve and maintain regulatory compliance and excellent pharmaceutical quality systems, to best industry standards.
If you need our help and support then please don’t hesitate to contact us.
Call: +44 (0)1244 980544
Email: enquiries@epic-auditors.com