We’ve designed our company’s laboratory and sterilisation units to be working hand in hand with our quality team, under one roof, at all times.
Once your products have been sterilised, Medistri will perform your Bioburden Testing, Bacterial Endotoxin (BET), Biological Indicators (BI) Sterility and Ethylene Oxide (EO) residual analysis in our GMP Accredited laboratory in Switzerland (also certified with ISO 17025) to analyse and demonstrate the safety of your sterile medical device.
Our Integrated In-House Infrastructure allows our customers to:
- Eliminate Logistical Complexities
- Simplify Operational activities.
- Simplify Supply Chain.
- Simplify Communications.
- Eliminate Uncertainty.
Discover how our pharmaceutical customers use Medistri's stack of integrated services ➝