Scilife Training | Practical compliance and inspection readiness for UK Pharmaceutical Quality Systems

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.

Training | Practical compliance and inspection readiness for UK Pharmaceutical Quality Systems

March 26, 2026 | 12:00H (CET)

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.

Register here for free

You’ll hear from Chris Homan, Pharmaceutical Quality and CMC Expert and Consultant and Angel Buendía, Scilife’s Knowledge Manager, will be moderating this session.

Strengthen your quality culture, learn from inspections, and ensure your organization is prepared to sustain compliance excellence over time.

REGISTRATION LINK: https://us02web.zoom.us/webinar/register/2417727158266/WN_KNBErm9FSNCjvuGIniVhHw