Cell & Gene Therapy
Reliability and efficiency are at the heart of patients' wellbeing and access to a personalized treatment. Don't take risks, trust Artel.
Cell & Gene Therapy
Reliability and efficiency are at the heart of patients' wellbeing and access to a personalized treatment. Don't take risks, trust Artel.
Miniaturized assays and low volumes leave no room for error
Cell and gene therapies have been employed to treat cancers, infectious diseases, neurodegenerative diseases or rare diseases. The research and development phase is critical, as efficacy, potency and safety of those new treatments must be ensured. Whether you are working with scarce patient-derived samples or dealing with low yields on your viral capsid harvest, you need your assays to work.
With Artel, you can take the liquid handling errors out of the equation! Artel PCS® and MVS® can help you ensure that the pipetted volumes are correct (even for volumes as low as 0.1uL) when you are prepping samples for your critical assays, such as qPCR, RT-PCR, NGS, ELISA, or HPLC.

John Derent
Global Account Manager
We're here to help
Low volumes and rare patient samples are tricky to work with, don’t take any risks! Use Artel. Reach out to see how we can help.
Scale up from manual to automation
Transferring your protocols from analytical development to manufacturing QC might include moving from a manual assay to an automated liquid handling process. The methods need to be reproducible across departments, platforms, instruments and operators, and assessed for accuracy and precision. Each step needs to be optimized to match your liquid handler, liquid class, and labware.
With Artel MVS and QualAssure® solutions, including Aqueous, PCRMix™ and SerumSub™, you can test your procedures, verify your results, make changes and validate your automation protocols quickly and easily, without wasting your reagents or samples.
Standardization and compliance are of the utmost importance
Partnering with academic institutes, universities, hospitals, CROs/CDMOs or disease centers is often needed in order to speed up a difficult process or reduce costs.
However, working with living specimens presents unique challenges due to the intrinsic variability of the starting materials, while the final product falls under high FDA scrutiny to follow GLP and GMP regulations. Producing lot-to-lot consistency throughout the manufacturing process can be challenging and is not always easy to accomplish.
With its instruments and volume verification services, Artel offers the first and only ISO 17025 accredited service and can help you achieve your internal quality goals and regulatory compliance.