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Pharmaceutical labs consider dissolution testing to be one of the critical steps in the drug development process. It makes an impact at almost every step of the journey, from early product development to late-stage quality control in commercial manufacturing. Given its importance throughout the course of drug development and manufacturing, dissolution testing has become a key concern for regulatory bodies – so the dissolution apparatus you depend on must provide the most accurate and reproducible results available.

To meet U.S. and E.U compliance guidelines, you need confidence in your compliance regiment, up and down the workflow. Working with the FDA/USP our teams have contributed to vibration limit evaluations and settings, including mechanical calibration and USP Performance Verification Test (PVT) services. Our OneSource services teams are staffed with engineers and consultants who know the ins and outs of dissolution testing and we provide technologies that produce clear, useful, and fully integrated reports so that you can stay compliant throughout the process. With 21 CFR part 11 software available, our state-of the-art UV/Vis instrumentation meets the needs of pharmaceuticals and manufacturing QA/QC analysts everywhere.