Bioanalytical Support Method Development & Bioanalytical Testing Services ABC Laboratories offers dose formulation and routine bioanalytical testing for preclinical through Phase III clinical trials. Our bioanalytical team has developed hundreds of proprietary methods across most drug classes and every biological matrix, and delivers expert quantitative analysis of drug and metabolites. Our approach to method development combines ingenuity with proven scientific practice. Our scientists apply extensive experience in HPLC-UV, LC-MS/MS, as well as ELISA and RIA techniques to deliver sensitive methods with the lower limit of quanitation (LLOQ). In addition to routine bioanalysis, we provide comprehensive analytical support for Human Mass Balance studies—in which we leverage in-house synthesis, dose formulation, and ADME expertise—as well as CMC support for Phase I radiolabeled studies. Sample Analysis-Routine Bioanalysis Dose formulation analysis Quantitative analysis of drugs and metabolites in biological matrices Interference Testing Immunoassays ELISA and RIA (125I) Sample Tracking and Storage Shipment of barcoded clinical kits to clinical site(s) Sample inventory and tracking by barcode Sample storage at -20°C or -80°C Dedicated staff for sample receipt & tracking Pharmacokinetic / Toxicokinetic Electronic Data Transfer Results in <48-72 hours for ascending dose trials PK/TK analysis This is another titlebar Analyst Empower 2 Win NonLin Sigmastat Daily back-up of raw data Detailed, customized reports & electronic reporting available ABC supports new drug, generic development and lifecycle management initiatives with expert bioanalytical testing services..