glp authorized

Good Laboratory Practice (GLP) is a quality system concerned with the organizational process and the condition under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported.

BioAdvice is a GLP authorized preclinical CRO which enables us to perform GLP studies according to OECD, FDA and Japanese guidelines.

We offer both regulatory studies (GLP) and Non-regulatory studies (non-GLP). The non-regulatory studies are carried out in the quality assured environment of BioAdvice’s GLP test facility but no study based QA-procedures are performed on the studies.