Simplify 21 CFR Part 11 Compliance with Sartorius Cubis® II

Staying compliant with FDA 21 CFR Part 11 regulations is critical in pharmaceutical and life science laboratories. Yet, meeting requirements for electronic records and electronic signatures can be complex without the right tools.

This free eBook provides a detailed compliance checklist showing how the Cubis® II MCA balance supports regulatory standards and helps labs maintain data integrity.

Inside, you’ll learn how Cubis® II balances enable you to:

• Ensure secure user management, audit trails, and electronic signatures.
• Generate accurate, complete, and tamper-proof electronic records.
• Protect data against unauthorized access or modification.
• Maintain traceability with automated time-stamped audit logs.
• Streamline inspections with exportable records in PDF, CSV, and Excel formats.