Events and webinars - Scilife Life Science Software
Scilife NV
FDA QMSR is now in effect—are you ready? Learn what the new regulation requires beyond ISO 13485:2016 and how to close gaps in risk management, documentation, and inspection readiness. A practical session to build a compliant, audit-ready QMS.
EMEA Office
Louizalaan 489
1050 Brussels
Belgium