EPiC’s Virtual GMDP Symposium 2025
Securing GMDP Compliance: Lessons from the Past, Innovations for the Future
‘EPiC’s view on current challenges and opportunities to help inform the future’
EPiC will be running our fifth full day virtual symposium on Tuesday 11th November 2025- featuring an esteemed lineup of former MHRA Inspector speakers. Join us as we explore the latest regulatory updates and guidance and provide insights into recurring compliance challenges and offer practical solutions to help you address current compliance gaps and build resilience to adapt and prepare for future regulatory changes facing the pharmaceutical sector.
We have completed a detailed review of the GMDP deficiencies and UK recall trends using MHRA published data and trend data from a wide range of audits and mock inspections performed by our consortium of former MHRA Inspectors to identify recurring issues that commonly result in inspection deficiencies and product recalls.
We will explore in detail the top deficiency categories and most common defect types for recalls in the UK to help you understand potential root causes and provide you with practical guidance and solutions to close compliance gaps and prepare for future regulatory changes.
Expect an interactive and informal experience carefully crafted to include:
- An update on pharmaceutical guidance and regulations
- EPiC insights on GMDP deficiencies and UK recalls
- The role of Quality Culture in moving from problem to solution
- Patient Information Leaflet Recalls – challenges and solutions
- Artificial Intelligence – practical strategies for adopting new technologies
- Data Integrity – changes ahead, but we can’t even get it right now!
- Stability under scrutiny – exploring out of specification trends
- GDP Masterclass – current challenges and future opportunities
Our panel of experts, drawing on their extensive knowledge and regulatory experience are committed to delivering a thought-provoking and informative event with an emphasis on providing practical guidance. Engage with them throughout the day and participate in a panel session to ensure all your pressing questions are addressed.
Our objective is to combine valuable insights using real world examples and collective experiences to provide the knowledge and offer practical solutions to help you buck the trend of recurring deficiencies and UK product recalls.
Who Is It for?
The event is ideal for pharmaceutical industry professionals in quality control, quality assurance, supply chain and production management, as well as Qualified Persons, Responsible Persons, and regulatory and compliance specialists involved in the manufacture and distribution of medicines.
What Will I Learn?
The event will provide the latest information and guidance on changing legislation and provide insights into recurring compliance challenges and explore in detail the top deficiency categories and most common defect types for recalls in the UK to help you understand potential root causes and provide you with practical guidance and solutions to close compliance gaps and prepare for future regulatory changes.
Through presentations, case studies and Q&A sessions, highlighting regulatory expectations, industry best practice and example scenarios, you will learn how to avoid common pitfalls that result in GMDP deficiencies and UK recalls of medicinal products.
Why Should I Attend?
- LEARN how to utilise practical solutions to overcome GMDP compliance challenges
- COLLABORATE with other Pharmaceutical Industry delegates
- CPD Continuous Professional Development to improve workplace skills and knowledge
- CONNECT with EPiC Directors and Senior Managers and expert Ex MHRA Inspectors
- ENGAGE in our presentations and panel discussions and hear Industry-focused case studies from our regulatory experts
- VALUE for money, presenting a wide range of topics from regulatory experts, with a ticket price of £350.00 + VAT per delegate
The Agenda
Coming soon!
The Speakers
Our event will feature an esteemed lineup of former MHRA Inspector and industry speakers – announcements coming soon!
Not available on the day? We understand your schedule may not allow you to access all the event sessions. A recording of the event will be made available after the event and will remain open 24/7 for 30 days.
Registered attendees will receive an email once the recordings and resources have been uploaded to the delegates area and can access the presentations whenever it is convenient during this time.
Continuous Professional Development
EPiC is a member of the CPD Certification Service which is recognised as the world’s leading and largest CPD accreditation service with over 25 years of experience.
An application will be made to accredit the event and award CPD points. If successful, Certificates will be sent to attendees within approximately 2-3 weeks after the event.
Testimonials
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For enquiries, please email: enquiries@epic-auditors.com
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