The MHRA, EMA and FDA are asking the same question: 'How you are achieving a state of GMP control in practice, not in theory?'
This complimentary webinar series explores the challenges of achieving robust GMP compliance across three sessions, each building on the last, designed to give you practical frameworks you can apply immediately.
We will explore why traditional GMP training often fails at the point of execution, what a true 'state of control' under ICH Q10 requires and how to equip you with strategies for consistent application and inspection readiness. The series concludes by examining the distinguishing practices of excellent GMP auditors and how to elevate auditing from a mere task to a powerful driver of quantifiable improvements and a thriving quality culture.
24 June 2026, 1:00pm - 2:00pm (BST)
Pharmaceutical companies invest significantly in training their workforce in GMP; yet ‘human error’ is still one of the highest causes of failure.
If training and compliance is an equilibrium, what are the ‘GMP Blind Spots’ that are preventing us from moving that equilibrium more to the right? How can we understand the human better so we can create instructions that really help?
In this webinar, we will analyse GMP, understand how to better apply training, learning and understanding of GMPs in a modern pharmaceutical workplace.
The session will cover:
- The 7 GMP blind spots most teams don’t know they have
- Why training to SOPs does not improve compliance and what to do instead
- How to apply a ‘process before procedure’ approach to SOP design
- Human error prevention techniques drawn from non-Pharma industries who are leading in error reduction
- The competence needs of the future and why diverse training approaches matter
Register here today.
8 July 2026, 1:00pm – 2:00pm (BST)
Henry Ford said over 100 years ago, 'Quality is doing the right thing when no-one’s looking'. A century later, the principle holds but the expectations have changed. The regulatory bodies now expect you to demonstrate a genuine state of control through evidence, not simply through documentation.
In this webinar, Peter Deegan dissects what true, consistent application of GMPs look like; how the workforce actually interacts with the ‘written PQS’ and how new approaches to learning theory are helping highly skilled people better comply with the routine; to show the state of control daily.
This session will cover:
- What an inspection-ready state of control looks like under ICH Q10
- Whether your GMP training plans are delivering consistency in compliance or simply generating records
- What inspectors really look for when they assess your state of control
- How other industries approach inspection readiness and what pharma can learn
- Risk-based process categorisation and know where to focus your effort first
- Whether right-first-time manufacturing is achievable and what it requires
Registration information to follow soon.
14 July 2026, 1:00pm – 2:00pm (BST)
When the auditor notifies you of an audit of your department, does everyone jump up excitedly, yelling 'Yes, this is fantastic! The auditors are coming'?
Are your self-inspections actually contributing to the value of your company? Saving time, effort, waste and improving compliance? Can you quantify a true reduction in inspection findings as a direct result of your internal audit programme?
In this webinar, Peter shows you how to make people genuinely value the auditor’s visit! How to quantify compliance-risk reduction and most importantly, how to demonstrate to senior management that the audit programme saves the company more money than the cost of auditing.
The session will cover:
- Top five auditor must-have skills, including how to think like an inspector, channelling the curious child within, preparing the auditee, dealing with difficult auditees, and writing incontestable audit findings
- Stop box-ticking and how to perform genuinely risk-based GMP internal audits
- Preparing for a regulatory inspection and how internal audits strengthen inspection readiness
- Human error and human behaviour, and what auditors should really look for
- True root cause and how auditors can drive lasting continuous improvement
- Training the auditee as well as the auditor
Registration information to follow soon.
Peter Deegan – Consultant and Tutor, RSSL
Peter is a highly experienced Pharmaceutical QA professional with over 30 years in GMP, ISO 9001 Quality Systems, auditing, and training. He has held key QA roles at major pharmaceutical companies, led a global training organisation, and specialises in Pharmaceutical Quality Systems.
Peter is renowned for his ability to cultivate a positive 'Quality Culture' across all organisational levels and is passionate about sharing his extensive expertise to empower others.
Can't make the live webinar? Don't worry - all of our webinars will be available on demand. Links to the on-demand versions will be available on this page shortly after the live event.
