Integrity and efficiency: AbbVie’s journey of building an integrated nonregulated bioanalytical laboratory

Author:

Wang Yue-Ting1ORCID,Maes Estelle M1,Heinle Lance1,Ruterbories Kenneth1,Doktor Stella1,Larsen Mary1,Olson Amanda1,Lee Andrew1,Van Handel Cecilia1,Ji Qin C1,Desino Kelly1,Jenkins Gary J1

Affiliation:

1. AbbVie, 1 North Waukegan Road, North Chicago, IL 60064, USA

Abstract

While bioanalytical outsourcing is widely adopted in the pharmaceutical industry, AbbVie is one of the few large biopharmaceutical companies having an internal bioanalytical unit to support nearly all its drug metabolism and pharmacokinetic studies. This article highlights our experience and perspective in building an integrated and centralized laboratory to provide early discovery and preclinical-stage bioanalytical support with high operational efficiency, cost–effectiveness and data integrity. The advantages of in-house nonregulated bioanalytical support include better control of data quality, faster turnaround times, real-time knowledge sharing and troubleshooting, and lower near- and long-term costs. The success of an in-house model depends upon a comprehensively optimized and streamlined workflow, fueled by continuous improvements and implementation of innovative technologies.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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