Quality for Life

CIBRO is compliant with FDA regulations for drug products and medical devices (21 CFR 211 & 21 CFR 820). We also adhere to customer corporate quality requirements. Our QA presence, which follows all projects from inception to completion, is consistently functioning in a FDA and cGMP regulated environment.

Our team is a network organization consisting of top chemists, microbiologists, lab technicians, QC inspectors, project engineers, validation technicians and regulatory compliance specialists. Working within a cGMP environment, they ensure FDA guidelines are met. The team clarifies requirements, secures specifications and takes pride in exceeding your expectations.

Any CIBRO employee who comes in contact with your product has received the appropriate cGMP training. CIBRO prevents problems and improves processes by analyzing statistical data and trends. Then, we recommend action when needed. These benchmarks allow us to maintain and improve strict product parameters.