Maidenhead, UK and Chapel Hill, NC – CROS NT today announced the go-live of its RaveX team in an extension of the company’s partnership with Medidata.
Under the partnership, CROS NT will offer its customers RaveX-the latest generation of Medidata’s industry-leading EDC system, Medidata Rave-as well as Medidata’s randomization and trial supply management (RTSM) system, Medidata Balance. The Data Management division in CROS NT offers Sponsors of clinical trials resources that are certified in the use of RaveX and Balance, on a project basis or in the form of functional service provision (FSP).
Services offered by the Data Management team include database build, data management and medical coding, all of which can be delivered from Europe, the U.S. and India. CROS NT has put in place a range of both statistical and data management technologies along with processes to give Sponsors oversight of the quality of monitoring and the quality of data coming from sites.
The extended partnership is part of CROS NT’s on-going development in operational capability. “CROS NT makes significant efforts to remain at the forefront of innovation. We are always seeking more efficient solutions for customers needing clinical trial services. Therefore, we are pleased to announce the extension of our partnership with Medidata, which is making great strides in the development of their own technology platform that allows us to better serve the needs of our expanding client base,” said Andrew MacGarvey, CEO of CROS NT. “This is especially important in the context of recent ICH E6 R2 guidelines, which call for a risk-based approach to clinical trials. We look forward to working with Medidata to deliver effective solutions for our customers,” he added.
“We’re thrilled to be expanding our relationship with CROS NT, a company that delivers high-quality clinical research services and understands the unique needs of its sponsors – from large pharmaceutical companies to small and mid-size pharma, biotech and medical device developers,” said Rick Bernstein, Medidata’s VP of global partnerships. “CROS NT’s further investment in the Medidata platform exemplifies its dedication to leveraging cutting-edge technology to support today’s most complex, data-driven research programs, and we look forward to further helping them advance their customers’ scientific goals.”
About CROS NT
Founded in 1992, CROS NT is a data-driven Contract Research Organization (CRO) providing services from feasibility to clinical study reporting for Phases I-IV and medical device trials. CROS NT’s services include regulatory consultancy, monitoring, data management, biostatistics programming & analysis, pharmacovigilance and medical writing – and accompanying eClinical applications (data visualization, EDC, IWRS, eCOA/ePRO etc.). All services are underpinned by strong clinical and biometrics project management with offices located in Europe, the USA and India. Visit CROS NT’s website at: www.crosnt.com
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Merck Launches Phase III Trials of Once-Monthly Oral HIV PrEP Candidate MK-8527
July 14th 2025In the new EXPrESSIVE clinical trial program, Merck will evaluate MK-8527, a once-monthly, oral PrEP therapy, in populations at high risk of HIV-1 infection, including adolescent girls and women in sub-Saharan Africa.
Baxdrostat Shows Significant Blood Pressure Reduction in Phase III BaxHTN Trial
July 14th 2025In the BaxHTN Phase III study, AstraZeneca’s baxdrostat demonstrated statistically significant and clinically meaningful reductions in systolic blood pressure in patients with uncontrolled or treatment-resistant hypertension.