DLR Bioanalytical Consulting has provided bioanalytical expertise to US and International Pharmaceutical and Biopharmaceutical companies, Contract Research Organizations and Institutional Financial Management Clients. We have greater than 30 years of experience planning and implementing GLP non-GLP drug development programs. We can provide scientific expertise in areas including method development and validation, method development strategies, method troubleshooting, root cause analysis, sample analysis, laboratory automation, matrix stability and ISR issues. We also provide business/regulatory expertise such as CRO selection, project management, laboratory/data audits, optimizing laboratory operations and work flow processes, data review and preparation and review of reports and SOPs.