With 20+ years of deep expertise, NorthEast BioAnalytical Laboratories LLC (dba, NorthEast BioLab) specializes in GLP and Clinical Bioanalysis Services for Biologics, Small Molecules, And Other Therapeutics. Our scientists and project team are trusted partners to hundreds of pioneering industry sponsors and renowned investigators and research leaders in the biotechnology sector. NorthEast BioLab is an independent, full-service, GLP/GCLP compliant, FDA audited, and DEA & CT State Schedule II-IV approved, Watson LIMS enabled facility. We continue to master method development, optimization, troubleshooting, and full method validation on Mass Spectrometric and Chromatographic Platforms (LC-MS/MS, HPLC-DAD/UV, etc.), Ligand Binding Assay (ELISA, Meso Scale Discovery, Luminex, Western Blotting, etc.), as well as qPCR. Our custom assay development services include Pharmacokinetics Analysis Studies (PK/TK/ADME/BABE), Toxicokinetic Safety Testing, Immunogenicity Assay (ADA & nAb), Cytokine Analysis, Biomarker Assessment, Cell-Based Assay, Biochemical Assay, Mechanism of Action (MoA) Investigations, etc. Established in 2003, our team comprises dedicated biologists and chemists on a quest to enable mission-driven biotech. These veteran team members have a proven track record and deep technical know-how to deliver your preclinical study and clinical assay development Contract Research Organization (CRO) services. Above all, our venture's spotlight is top quality and industry-leading turnaround at competitive pricing. Thus, our entire team would happily assist you with effective strategies to meet the stringent timelines of various milestones throughout your drug development life-cycle. Speak To Our Scientists Today To Expedite Your Bioanalytical Assay Development, Validation, and Sample Analysis!