BioAnalytical Services

Experience

With over 30 years experience in BioAnalytical methods development and validation, preparation and review of client protocols, methods, reports, and analysis of pharmaceutical compounds in biological fluids, CRL's dedicated team has proven success in critical projects.

CRL’s BioAnalytical scientists have a firm understanding of quality assurance principles and good laboratory practices. They are skilled with cutting-edge laboratory procedures and equipment, specializing in LC/MS-MS and with solid phase extraction and high-throughput sample processing.

Our experience includes LC/MS-MS method development, BioAnalytical methods development and validation for lower molecular weight pharmaceutical compounds and for larger molecular weight peptides.

Our expertise in meeting FDA/GLP guidelines and our experience preparing and reviewing client protocols, methods, and reports helps you with complex and highly technical processes, cut costs, and decrease time-to-market.

Additionally, our scientists' experience developing quality systems and internal audit programs helps ensure compliance of work with federal regulations, internal quality standards, and critical schedules.