Uploaded October 2022 | Updated September 2026, 5 hours ago
Learn how to align microscopic analyses 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
Learn how to align microscopic analyses 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
