Learn how to align microscopic analyzes in the pharmaceutical or medical device industry with GMP or GLP. You will also learn about compliance with regulations such as FDA 21 CFR Part 11 or Pharmacopoeia. You can easily validate your processes and make them GMP compliant. When it comes to the qualification process, our ZEISS experts will support you every step of the way.

You benefit from:

– Configurable user management
– Guided workflows
– Digital signatures
– A complete audit trail
– And checksum protection of your data

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