Why Regulatory Refresher Training Needs a Makeover
If your annual refresher training feels like déjà vu, you’re not alone. Many organisations are stuck in a cycle of recycled slides and outdated examples - missing the chance to spark real learning and protect quality. This blog is a personal reflection on what’s going wrong, why it matters, and how we can do better.
Ready to shake up the status quo and make training meaningful again? Let’s rethink it - one conversation at a time.
Preclinical Data Integrity & GLP Compliance: Why Sponsor Oversight Matters for Successful Drug Development
Many sponsors assume GLP certification is enough to guarantee data reliability - but without proper oversight, hidden risks in early-stage research can undermine regulatory submissions and programme success. This article explores how to spot oversight blind spots, meet regulatory and industry expectations, and safeguard your scientific decisions with confident, strategic QA.
From Scientist to Leader, Auditor to Quality Visionary: The Untaught Skills That Define Success
Transitioning from technical expert to impactful leader requires more than scientific skill. Discover the essential but often overlooked leadership competencies needed for success in pharmaceutical and QA roles, and learn practical strategies to bridge the gap.
Unlocking Excellence: How Outsourcing Your Audit of QA Could Transform Compliance
Auditing your QA function goes beyond ensuring compliance - it’s an opportunity to uncover inefficiencies, optimise processes, and drive meaningful organisational value. Discover actionable strategies and insights that position QA as a cornerstone of compliance and innovation. This post delves into the challenges and opportunities of a strategic QA audit, with a free guide to help you maximise its impact.