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CUSTOM TOXICOLOGY AND MICROBIOLOGY STUDIES

Pacific BioLabs offers custom research and testing services in support of drug and medical device discovery and development. Our scientific staff can assist in the design and implementation of studies that meet specific compound or product development needs, while maintaining the required level of regulatory compliance. 

Full Development Cycle Support

Our support of client needs spans the life cycle of drug and device development, from implementation of client-specific pharmacology of efficacy models (non-GLP), to modification of standard toxicology studies in support of regulatory submissions (GLP), to support of manufacturing activities through bioassay for stability and microbiological test procedures for lot release (cGMP). All of these activities can be customized to suit the specific needs of a particular development project.

Pacific BioLabs supports these custom studies in multiple ways. We work closely with clients to transfer and implement their testing procedures at Pacific BioLabs and we also develop and implement client-specific procedures using our own highly qualified staff.

Certified and Accredited Services

All in vivo test procedures at Pacific BioLabs are vetted through our IACUC (Institutional Animal Care and Use Committee) and are conducted in our AALAC-accredited and USDA-inspected animal facility.