Resource overview
The Cubis®️ II balance, with pharma package, contains all the technical controls to support compliance with common regulations. Full compliance can be achieved with additional procedural controls and systems for long-term data storage. This checklist helps you to keep an eye on relevant details of the regulation. In addition, you can see how Cubis®️ II is offering solutions to be fully pharma compliant.
Key takeaways
- Get detailed insights into FDA’s 21 CFR Part 11 standards for electronic records and electronic signatures
- Practical guidelines for setting up systems that meet regulatory requirements
- Knowledge about the Cubis® II MCA system’s capabilities
- Importance of validating laboratory systems and maintaining documentation for regulatory compliance audits
Resource details
- Document type: ebook
- Page count: 10
- Read time: 22 minutes
