FDA 21 CFR Part 11 Microscopy Solutions in the Medical Industry


Date: Thursday, July 13, 2023
Time: 2:00 PM Eastern Daylight Time
Duration: 1 hour

It is critical for microscopy users to gain traceable workflows through seamlessly integrated microscopy hardware and software to fulfill the requirements of regulated industries. Understand how inspections on light and scanning electron microscopes can be made compliant. GxP is all about making processes more secure, traceable, and compliant for medical regulations.

  • Learn how to make microscopy processes compliant to FDA 21 CFR Part 11 Regulations
  • Hear how hundreds of Medical and Pharmaceutical customers were served
  • See how the ZEISS ZEN core Toolkit GxP can be used with all ZEISS Microscopes
  • Understand the validation process ZEISS uses to support our customers with regulated applications

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Roger Landolt, MBA
Senior Software Sales Manager – Regulated Industry

Roger has over 10 years of experience with ZEISS Software products for Medical and Pharmaceutical applications. He provides support and consultation to customers with their microscopy projects in regulated environments.
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