Virtual Compliance Symposium 2023

EPiC will be running an online symposium on Tuesday 5^th December 2023

The theme is Beyond the Basics: Mastering GMDP Compliance & Inspection Readiness

ABOUT

EPiC is proud to present our full-day virtual symposium 2023 event featuring an esteemed lineup of former MHRA Inspector speakers. Join us as we delve into the latest updates, guidance and regulations shaping the pharmaceutical industry.

We will explore crucial topics that include recent updates to industry guidance and regulations, inspection readiness, deficiency data interpretation, innovation and ATMPs, risk assessment and the revised ICH Q9 and GDP trends and developments, as well as running an Annex 1 workshop. Our objective is to provide you with invaluable insights on how to navigate the ever-changing regulatory environment that governs medicinal product manufacturing, and supply.

Expect an interactive and informal experience carefully crafted to promote engagement. Our panel of experts, drawing on their extensive knowledge and regulatory experience are committed to delivering a thought-provoking and informative event. Engage with them throughout the day and participate in a panel session to ensure all your pressing questions are addressed.

Discover how our expertise can take you beyond the ‘basics’ and propel your organisation towards excellence in pharmaceutical manufacturing and compliance.

 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 give you insight into Mastering GMDP Compliance and Inspection Readiness. Through presentations, workshops, and Q&A sessions, highlighting regulatory expectations, industry best practice and deficiency trends, you will learn how to improve your PQS, ensure you are inspection ready, and gain essential advice on maintaining the highest standards of compliance.

 WHY SHOULD I ATTEND?

• LEARN how to master GMDP Compliance and Inspection Readiness
• NETWORK 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 Workshops and hear Industry-focused case studies from our regulatory experts.
• VALUE for money, presenting a wide range of topics from regulatory experts.

  OUTLINE AGENDA

 Tuesday 5^th December 2023

(09.00 to 5.00 GMT) to include:

• Recent Updates to Guidance & Regulations
• How do you know you are Inspection Ready?
• Deficiency Data-Interpretation & Root Cause Analysis
• Innovation and ATMP Panel Discussion
• Annex 1 – Contamination Control Strategy (CCS) / Gap Assessments – Workshop
• ICH Q9 (new revision) – Risk Assessment
• MHRA Update: Speaker requested.
• GDP Hot topics – challenges faced by RPis, The Windsor Framework update, GDP inspection approaches.
• Q&A Panel Session

CPD

An application has been made to accredit the event and award CPD points. If successful Certificates will be sent to the email address, you registered within approximately 2-3 weeks after the event.

Tickets cost £300 + VAT.

If you have any questions, then email EPiC at enquiries@epic-auditors.com

To Register and book your place click:  Click here to register

 

 

 

 

Pharmaceutical Training and Education You are only as good as your people. NSF offers education programmes that will change behaviours, improve performance and “future proof” your organisation. Training can be delivered in-person, online via a live instructor-led virtual classroom or as self-paced eLearning. We can customise our courses to your requirements. Virtual Instructor-Led Training We redesigned our courses to suit virtual learning, making the best use of technology to enhance interactivity. Our online delivery platform utilises features such as polls and break-out rooms to promote discussion and knowledge transfer while working through tasks and case studies. Many of our virtual courses require elements of self-paced learning to be completed both before and after the classroom. This is managed through our learning management system and allows participants to access and download course information electronically. Self-Paced eLearning Our eLearning supports and complements our traditional training. It includes short, targeted, highly focused “how-to” sessions on common industry themes as well as introductions and overviews on topics essential for those new to the industry. Start your learning Health Sciences Journal Sign up to NSF’s free digital Journal, full of valuable learning resources from industry experts as well as guest Q&A articles, regulatory updates, and all the latest NSF news – don’t miss out! Sign up and view the latest edition “I thoroughly enjoyed completing both elements of this course – self-paced eLearning and the in-person virtual instructor-led training – and would highly recommend it to my colleagues. I have gained a heightened awareness of virtual and remote auditing, which could prove invaluable in the current crisis.” – Debbie Evans Download our pharma app: Apple App Store | Google Play For further information on our consulting, auditing and training services, visit our website, or contact us at pharmamail@nsf.org.