Practical compliance and inspection readiness for UK Pharmaceutical Quality Systems
Is your UK pharma quality system ready for inspection? 🔍
Rising MHRA scrutiny.
Growing data integrity expectations.
Increasing regulatory pressure.
Join our free webinar to learn practical strategies to strengthen compliance and maintain inspection readiness.
🎤 Featuring Christopher Homan, Pharmaceutical Quality and CMC Expert
Prepping for inspections in today’s UK regulatory environment is becoming increasingly complex: the heightened scrutiny, rising expectations, constant pressure on your systems…
If it feels like your pharmaceutical quality system is under a magnifying glass, join this webinar, where our regional regulatory partner will share practical strategies to strengthen compliance and maintain inspection readiness, without overcomplicating your system.
We’ll show you how to:
- Understand current UK and EU regulatory expectations and their impact on your PQS
- Address key quality system considerations for growing pharma and biotech companies
- Navigate current MHRA, FDA, and EMA inspection trends, including data integrity focus areas
- Maintain inspection readiness through practical, sustainable approaches
You’ll hear from Christopher Homan, Pharmaceutical Quality and CMC Expert and Consultant and Angel Buendía, Scilife’s Knowledge Manager, will be moderating this session.
📅 March 26th, 2026 | 12:00H (CET)
Strengthen your quality culture, learn from inspections, and ensure your organization is prepared to sustain compliance excellence over time.