Our expert toxicologists can help you design a cost-effective toxicology program to screen candidate drugs, assess formulations, and get your product into the clinic. PBL's flexible scheduling and fast turnaround help you meet your drug development milestones - on time! And our well designed protocols and well documented reports help speed regulatory review of your submission. Clients have used PBL studies to support hundreds of INDs, NDAs, and PLAs.
PBL's QA/QC testing services include a broad array of microbiological, in vitro and in vivo procedures to support cGMP manufacturing of pharm/biopharm products.
PBL has an outstanding track record in FDA GMP and GLP inspections. Our robust GMP and GLP compliance programs combine with a rigorous system of quality management to ensure the technical and regulatory quality of your studies. |
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"Our new product was introduced today and was received extremely well. Pacific BioLabs' hard work and timely service had much to do with its success "
- Product Manager
San jose , CA |
