Скачать или смотреть How to integrate process monitoring into your medical device production

Medical device manufacturers now face some of the strictest requirements in any industrial sector. 100 percent traceability of quality-relevant manufacturing data must be ensured, and producers must also meet compliance requirements for the qualification of measurement technology and process validation based on standards, guidelines and directives such as GAMP 5 or EU GMP Annex 11.

Kistler now invites you to a webinar when two of our experts will present solutions to the problems of compliance in the medtech sector. Stephan Vogel, Head of Business Development and Martin Lack, Head of Product Management at Kistler Instrumente GmbH, Sindelfingen (Germany) will explain how integrated process monitoring can help you overcome these challenges. They will introduce you to the basics of deploying measurement technology directly in the manufacturing process. Then, they will focus on key issues such as:

• Choosing the best sensor for your specific purpose
• The new maXYmos TL ML process monitoring and control system, specifically designed for the medtech industry:
– What new functions does it offer you?
– How does it ensure even better integration into medical lines?
• Inline calibration of measuring chains: how to meet the mandatory requirements

This deep dive combines practical insights with a clear explanation of the concept of integrated process monitoring. The webinar will conclude with a Q&A session when your hosts will gladly share their experience and know-how with you.

Let the global leader show you how transparent and traceable monitoring can optimize your medical device production! Register now for our webinar on integrated process monitoring for the medtech industry.