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A virtual biotech company chose Covance to conduct two Phase III clinical trials for a new antibiotic treating life-threatening skin infections, such as methicillin-resistant staphylococcus aureus (MRSA).

A top-5 pharmaceutical company partnered with us to provide field reimbursement management (FRM) services for their autoimmune infusion therapy program. Learn more about how we played a critical role in facilitating enrollment and stakeholder satisfaction.

A large biopharmaceutical company was running two Phase III trials for a novel Hepatitis B treatment. Their global studies included participants in China, and the company asked Covance to support their external laboratory testing for this cohort.

The Xcellerate® Site List Tool is the only analytics tool in the industry that aggregates actual investigator recruitment performance data from over 50% of all industry-sponsored trials conducted globally to maximize the likelihood of reaching patient recruitment milestones on time.

The integrated summary of safety (ISS), integrated summary of efficacy (ISE) and Study eSubmission deliverables are considered key components of a New Drug Application (NDA) for the U.S. FDA as well as other regulatory agencies around the world.

The Xcellerate® Protocol Design Tool is the only analytic tool in the industry that leverages de-identified diagnostic data from one of the world's largest sources of lab result data. It synthesizes 30 billion+ diagnostic test results from over 150 million people across more than 5,000 assays to improve the likelihood of recruiting success.

ICCS 2020 -- With the advances made in new cancer therapies, many CLL (Chronic Lymphocytic Leukemia) patient remission rates are significantly improving.

CORESTA Congress 2020 -- The battery of regulatory assays currently used to assess the toxicity of aerosol exposure are limited in their ability to identify changes at the cellular and molecular level. This has prompted a shift towards a more holistic systems biology approach when assessing the effects of exposure to potential toxicants.

CASSS AT Europe 2020 -- Forced degradation studies involve subjecting a putative drug substance or drug product to elevated chemical and environmental stress. This allows product degradation pathways and potential impact on efficacy or safety to be understood. It is also used to challenge the sensitivity and specificity of analytical methods.