Scaling a CDMO often requires more than additional manufacturing capacity. The greater challenge is building the analytical capability, consistency, and operational alignment needed to support more programs, more complexity, and higher sponsor expectations.
As your operations become more fragmented, you face longer development timelines, more difficult tech transfer, greater compliance risk, a less consistent sponsor experience, and a rising cost to serve.
Agilent helps you remove these barriers with a standardized analytical ecosystem of instruments, software, and services designed to help you grow your business with more speed, control, consistency, and stronger economics.

We use several Agilent HPLC systems in our lab, including the 1290 Infinity III, 1290 Infinity II, 1260 Infinity II, and 1260 Infinity to support our RNA development and analytical workflows. We routinely use these systems for RNA characterization and purification using different chromatographic methods, including IP-RP HPLC and SEC.
The systems have been reliable for both routine testing and method development, especially when we need consistent performance across different RNA samples and projects. The flexibility of having multiple Agilent platforms also allows us to accommodate different methods and increasing sample workloads while maintaining good reproducibility between runs. This helps us make development decisions quickly and with confidence, while maintaining the quality and turnaround times needed to support our customers.
Shambhavi Shubham, PhD
Sr. Manager, RNA R&D
GenScript, a Global CRDMO
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