External Clinical Trial Lab Testing Reduces Costs While Promoting Data Quality and Consistency

Covance, one of the world’s largest and most comprehensive drug development companies, has announced the launch of external laboratory management services, a new offering that provides biopharmaceutical companies with a comprehensive management solution for external laboratory testing associated with clinical trials.

Covance’s external laboratory management services are designed to maximise the quality and integrity of clinical study data by ensuring that laboratory testing is seamlessly managed for the client along with services provided by a central laboratory. These services include laboratory selection and qualification, auditing, vendor management, contracting and data cleaning. The new

Covance services will be managed by a dedicated team within Covance’s central laboratory services and complement the company’s capabilities in central laboratory testing, biosample management and data services, resulting in a streamlined solution that frees pharmaceutical companies from the challenges of managing multiple laboratory testing vendors.

By leveraging economies of scale and minimising duplication of effort, Covance’s external laboratory management services can reduce the cost of managing external testing by as much as 65% when compared with clients’ in-house management of the process. In addition, improved data cleaning can decrease the length of trials, accelerating data lock.

“Through our external laboratory management services, ISO-15189 accreditation and understanding of the regulatory landscape, Covance is uniquely positioned to enable our clients to meet higher levels of data scrutiny from agencies around the globe,” said Gary Paul, Global Director of Quality Assurance for Covance Central Laboratory Services. “As the pioneer of the central laboratory model, this new offering further establishes Covance’s position as a leader and innovator in clinical trials testing and sets a new industry standard for the management of data quality.

Paul Kirchgraber, Vice President Global Laboratory Operations & Medical Affairs, added: “By providing an enhanced laboratory data solution that reduces regulatory risk and lowers drug development cost, we enable our clients to focus on their core competencies, ultimately accelerating development and commercialisation timelines.”

In recent years, increased regulatory scrutiny of clinical programmes has led to the creation of an industry standard, ISO 15189, to help control laboratory data consistency and quality. While the majority of clinical trial testing occurs at central laboratories, an increasing percentage of trials include at least one specialised test that is sent to an external laboratory. Covance’s external laboratory management services are designed to help biopharmaceutical companies address their growing testing needs while mitigating potential risks, increasing data consistency and decreasing the cost and time associated with clinical development. More information about Covance’s central laboratory services can be found at www.covance.com/products/clinical/central-lab.

Covance Inc., +41 798236706, sabine.schneidernash@covance.com, www.covance.com.