GxP stands for “Good x Practice” and is a set of quality guidelines and regulations that apply to the pharmaceutical industry. The “x” in GxP represents the specific field that the guidelines apply to, such as manufacturing, distribution, laboratory, clinical, or documentation. The goal of GxP is to ensure that pharmaceutical products are safe and meet their intended use by maintaining quality throughout all stages of the product’s life cycle.
“Transform Your Training”-5 Top Tips for Implementing an Effective Training Program Article By Vicki Pike, Operations Manager for EPiC Auditors Training is essential in the pharmaceutical industry for several key reasons. Proper training helps maintain high standards of product quality and…
EPiC Auditors Virtual Symposium 2024: From Complaint to Compliant: A Practical Guide to Overcoming Current GMDP Challenges Join us for EPiC’s fourth annual virtual symposium on Thursday, 28th November 2024, titled “From Complaint to Compliant: A Practical Guide to Overcoming…
GXP Compliance Challenges The constantly evolving landscape within the pharmaceutical industry presents a myriad of challenges, especially when it comes to compliance. Across the GXP’s the range of compliance areas is vast and varied. Your experiences and insights are invaluable…
Ensuring Excellence in GXP Compliance: Discover the EPiC Difference Through Our Client Testimonials Our mission has always been to foster product quality, patient safety, and ensure the highest regulatory standards. But don’t just take our word for it—let our clients…
“Keep Calm and Be Prepared” – 5 Top Tips for Inspection Readiness Article By Michelle Yeomans, Operations Manager for EPiC Auditors Judging by the number of enquiries we are receiving to provide ex MHRA Inspectors to assist with inspection readiness…
Our expert consultants, Darren Jones and Philip Rose have returned from a successful on-site audit in Indore, India. Working alongside a highly skilled team, they exemplified EPiC Auditors Ltd’s unwavering commitment to delivering GXP auditing excellence worldwide. During the rigorous…
“Mind the Gap” – 5 Top Tips for Improved Self-Inspection Article By Michelle Yeomans, Operations Manager for EPiC Auditors During our time as MHRA Inspectors and now as pharmaceutical consultants, at EPiC we routinely see non-compliant sites i.e., those referred…
Serious about Making Pharmaceuticals? Our Directors Richard Andrews and Darren Jones will be joining GMP Healthcare Ltd on stand 220 at this year’s Making Pharmaceuticals Conference in Coventry on the 25th – 26th April 2023. As the largest Pharmaceutical Event in the UK, it covers everything…
5 Top Tips for Implementing Effective Knowledge Management Practices Article By Michelle Yeomans, Operations Manager for EPiC Auditors At the EPiC Autumn Compliance Seminar, I delivered a presentation outlining the direction of travel in demonstrating compliance (Session 1. GMP Seminar…
MHRA Inspectorate Blog has recently published Part 2 in the Compliance Monitor Process series with further information about the Compliance Monitor (CM) role and application process. The blog can be found here: Compliance Monitor Process (Part 2)– CM role and…