Reproducibility is Key

Every lab has protocols that only one researcher or technician (or, perhaps, no one at all!) can reliably reproduce. There must just be something about that person's lab technique, pipetting angle, stirring form, or general aura that makes it work. You could have other people work with them, observe them, take notes, video tape them. Or you could do the most reproducible, cost-effective thing possible: automate it! We can work with your "golden hands" practitioner to develop custom equipment, automate existing equipment, or modify commercially available equipment to reproduce what they do. The same way. Every time. No more pages and pages of protocols, no black magic, minimal variation. Then, your green-thumb lab jockey will have the time he/she needs to search for new protocols to conquer.

Small-Scale Automation for Bio/Pharma

For some time now, large-scale production in the pharmaceutical industry has been highly automated. Large vessels turn a few grams of something into kilograms upon kilograms of precious life-saving compounds. The air-tight seals, tight temperature controls, and carefully thought-out process interlocks make this happen quickly, repeatably, and with the minimal possible contamination.

Consider the state of automation in the R&D lab, or in pilot production environments. It has long been realized that things like vortex stirrers, centrifuges, and iso-temperature baths help enable researchers to do more with their cell lines or syntheses. However, what about that next step in automation? There is probably no commercially available system to do exactly what you need. But if you could benefit from the 24X7X365 throughput and complete reproducibility offered by an automated solution, kDy Automation Solutions is just the ticket to make your process into something that can run unattended. Or can email or page or send pictures or even offer remote control to lab personnel in the case of an emergency or adverse event. We will stick with you through the equipment validation(IQ,OQ,PQ), process validation, FDA and ISO requirements, and beyond.