Get ready for FDA's QMSR Final Rule with Scilife

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Navigate change and ensure regulatory compliance

In this free session, Angel Buendía (Knowledge Manager) and Sara Kong (Product Specialist) will provide you with an overview of key changes crucial for life sciences compliance and operational efficiency, and how Scilife can make your QMSR management seamless.

What you’ll learn in this session

In this session, you’ll see a practical demonstration of how: 

• Scilife's Document Control solution streamlines QMS process determination and documentation alignment with regulations.
• Scilife's Change Control solution facilitates recording and evaluating process and device changes seamlessly.
• Scilife's KPIs solution empowers comprehensive process monitoring, measurement, and analysis for improved quality management.

Speakers