Global Pharmaceutical Consultants GXP Consultancy

FAQ’s

Who are EPiC?

EPiC are a team of former MHRA inspectors and industry experts providing specialist GxP compliance services to the pharmaceutical, biotech, and healthcare sectors. We help protect patients by helping you meet regulatory expectations and improve quality systems.

What services does EPiC offer?

EPiC offer a wide range of services including GxP audits, mock regulatory inspections, gap assessments, training and education, remediation support, and contract QP/RP/RPi services. See our services page here: Services

What makes EPiC different from other compliance consultancies?

The EPiC team includes former regulators and senior industry professionals with real-world experience. We combine regulatory insight with practical, risk-based solutions tailored to your business.

Who do EPiC work with?

EPiC support pharmaceutical manufacturers, biotech companies, advanced therapy medicinal products (ATMPs), clinical trial sponsors, wholesalers, and hospital manufacturing units across the UK and internationally. Our consultants are familiar with UK and international regulatory frameworks such as EMA, FDA, and PIC/S.

Can EPiC help prepare for an MHRA or FDA inspection?

Yes. EPiC offer mock inspections, inspection readiness training, and gap assessments to ensure your team and systems are fully prepared for regulatory scrutiny.

How can EPiC help improve our pharma compliance culture?

EPiC provide tailored training, mentoring, and strategic advice to embed a culture of quality and compliance throughout your pharmaceutical manufacturing organisation from the top down.

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