What FDA QMSR requires from your QMS and how to get ready
QMSR is here, and early inspections are already exposing gaps.
If your QMS hasn’t evolved, this is the moment to take a closer look.
In this free session, learn what FDA inspectors are focusing on and how to close critical gaps in risk, documentation, and QMR processes.
QMSR is here, but is your QMS truly ready for it?
Many companies assume their current systems will hold. But early inspections are already showing gaps, and expectations are becoming more structured and less forgiving.
In this session, we’ll unpack what QMSR really requires in practice, and where companies are most at risk.
We’ll explore:
- Where companies are already falling short under QMSR
- What FDA inspectors are focusing on in early enforcement
- How to close gaps in risk management, documentation, and QMR processes
- How to move from reactive compliance to inspection-ready operations
- How a modern eQMS can support QMSR readiness without increasing operational burden
You’ll hear from Jennifer Mascioli, MedTech expert, Angel Buendía, Scilife’s Knowledge Manager and Santosh Paragond, Account Executive, who will show you how to translate QMSR requirements into sustainable, compliant operations.
📅 April 23rd, 2026 | 11:00H (CET)
Join us to make sure your QMS is ready for what QMSR demands!