18 Frequently Asked Questions (FAQ)
On January 1st, 2022, the new European Pharmacopoeia (Ph.Eur.) Chapter 2.1.7, on analytical balances went into effect.
The Ph.Eur. is the legally binding reference for all pharmaceutical companies placing pharmaceutical products in the market of European member states.
Download this guide to find out the answers to these commonly asked questions about Ph.Eur. compliance:
- What are the requirements of Chapter 2.1.7 concerning the calibration of a balance?
- What are the requirements on repeatability and sensitivity?
- How often should performance checks be conducted?
- How does the Cubis® II laboratory balance support compliance with Chapter 2.1.7?
