Sample Prep for Quality Control
From solvent to syringe—confidence in every analytical step.
In the biopharmaceutical and medical device industries, quality control (QC) is non-negotiable. Each drug or device must be demonstrably safe, pure, potent, and consistently manufactured. Sartorius delivers a fully integrated sample preparation workflow to support trace-level detection and data integrity across HPLC, LC-MS, IC, and ICP-MS applications.
Four steps. Total confidence:
- Preparation of Solvents
- Up to 80% of HPLC issues stem from water impurities.
- The compact Arium® Mini system delivers ultrapure Type 1 water for mobile phases, buffers, and diluents—essential for accurate separation and detection.
- Preparation of Standards
- The Cubis® II balance with pharma package ensures FDA 21 CFR Part 11 and ALCOA+ compliance.
- YAPP16 software guides users through single or multi-component dosing with built-in sample, solvent, and concentration databases.
- Liquid Handling
- Picus® 2 electronic pipettes offer protocol-guided precision and ergonomic ease.
- Tacta® mechanical pipettes and Optifit/Safetyspace® tips guarantee secure fit and reproducible results for every volume transferred.
- Filtration
- Claristep® Station filters 8 samples (60–600 µL) in parallel—no power, pumps, or syringes needed.
- Minisart® PP syringe filters ensure compatibility and low extractables for the cleanest possible sample injection.
Designed for compliance. Engineered for consistency.
From ultrapure water and gravimetric accuracy to ergonomic pipetting and high-recovery filtration, Sartorius enables QC teams to optimise workflows, improve traceability, and meet the rising demands of global regulatory agencies.
Download the full workflow guide and upgrade your QC sample prep today.