|Articles|September 11, 2012

ICON Expands its US and UK Bioanalytical Laboratories

ICON plc

, a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, today announced the expansion of its US and UK bioanalytical facilities to meet the growing demand for biomarker and cell-based assay services.

ICON has increased its bioanalytical laboratories in Whitesboro, New York, and Manchester, UK, by 7,000 and 4,000 square feet respectively. The expansions allow ICON to house dedicated immunoassay laboratories at each facility for biomarker testing and cell-based assays. Operating since 1988, ICON’s Whitesboro facility already features multiple wet laboratories and instrument laboratories for small and large molecules, including a specially designed hazardous lab for the analysis of HIV & Hepatitis B infected samples. Similarly, ICON’s Manchester laboratory has provided bioanalytical support for both small and large molecule studies for almost 30 years and is located close to ICON's hospital-based Clinical Pharmacology Unit in Manchester.

“We have expanded our bioanalytical facilities to provide the necessary scale to support the ever-broadening range of testing services required by our sponsors,” commented Brian O’Dwyer, Senior Vice President of Global Bioanalytical Services, ICON Development Solutions. “In particular, the expansion of our dedicated biomarker testing laboratories allows us to support biomarker development programs across multiple testing platforms globally.”


Related to this article

The Human Side of Clinical Trials: Why Fuzzy Mental Models Undermine Clinical Trial Execution
In Episode 3 of The Human Side of Clinical Trials, hosts Brian S. McGowan, PhD, FACEHP, chief learning officer and co-founder of ArcheMedX, Inc., and Kelly Ritch, chief operating officer of ArcheMedX, Inc., speak with Jason Riis, PhD, CEO and chief behavioral scientist at Behavioralize, about why a well-written protocol doesn’t always translate into consistent execution, and how designing for the way people actually think and learn can reduce site burden and the need for costly unlearning.
© putilov_denis - © putilov_denis - stock.adobe.com
Real-time clinical trials require standardized digital data capture at the point of care through scaled eSource-EDC-EHR integration, but progress stalls because competing standards lack regulatory enforcement and one-off system integrations cannot scale beyond single studies without industry-wide alignment and legal clarity on data ownership.