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

Kistler now invites you to a webinar in which two of our experts will present solutions to the challenges 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 introduce you to the basic principles of directly using measuring technology in the production process. They will then focus on important issues such as:

• Choosing the best sensor for your specific purpose
• The new maXYmos TL ML process monitoring and control system, specially designed for the medtech industry:
– What new features does it offer you?
– How does it ensure even better integration into the 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 concludes with a question and answer session in which your hosts will be happy to share their experience and know-how with you.

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

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