Promoting Quality & Efficiency for Bioprocessing

Once your candidate drug is ready for human testing, it undergoes a rigorous progress where it is closely evaluated for safety and efficacy in treating, preventing, or diagnosing a specific disease or condition. Because the safety of trial participants is the most important consideration, all testing occurs in FDA-supervised phased clinical trials, along with further assays to characterize absorption, distribution, metabolism, excretion, and toxicity.

Consistency, reproducibility, and reliability are critical to accelerating your drug discovery and development journey from target identification through scale-up manufacturing. In order to maintain the highest quality standards and productivity, choose products that automate your workflow, and reduce hands-on time, so you can focus on your most critical tasks.

Translational Research takes scientific discoveries made in the laboratory, the clinic, or in the field, and transforms them into new medical treatments and approaches that improve human health. The process of applying discoveries generated during lab and preclinical research to human clinical trials, requires work to ensure quality including validating biomarkers, optimizing therapeutics for safety and efficacy, and determining the best purification processes and formulations for human trials.