When developing the next generation therapeutics or vaccines, reliability and speed are at the heart of your success. Our liquid handling verification systems are helping biopharmaceutical labs get ahead and stay ahead.
Shortening time to market is not only critical to meet patients’ needs, but it is also essential to stay ahead of competitors. Automating and taking control of your assay workflows can make the process more efficient. With Artel MVS and PCS, you can check your automated liquid instruments as often as needed, identify trends before failures happen, and avoid costly downtime.
Regulatory requirements in the biopharmaceutical industry are unique and demanding. The production of any therapeutics, vaccines or other drugs needs to comply with FDA 21 CFR, including GLP, GMP and other ISO standards. These regulations help provide confidence in the quality, safety and efficacy on the market. When it comes to your automated liquid handlers, pipettes, and personnel, we can help reduce variability from lot-to-lot, lab-to-lab and site-to-site across a global organization by easily verifying accuracy of dispensed volumes.
Learn more about how liquid handling verification can be utilized to optimize your workflows by checking out our educational resources below.
We will work with your laboratory to understand your volume transfer testing parameters and requirements. Our team provides the tools and experience to indiscriminately measure volume transfer variability for nearly all liquid handler makes/models.
Learn moreMelinda Gold
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Product Manager, Artel Product Portfolio
