Global Biopharma Adds Medidata Clinical Cloud® to Enhance Its Clinical Trial Data Management Capabilities
NEW YORK, N.Y. – February 10, 2016 – Medidata (NASDAQ: MDSO), the leading global provider of cloud-based solutions for clinical research in life sciences, today announced that Celgene Corporation has expanded its eight-year technology relationship with Medidata to add the Medidata Clinical Cloud® as its enterprise technology platform for all clinical trials worldwide.
To drive therapeutic excellence in the interest of patients through a sustainable pipeline of cancer and inflammatory disease treatments, Celgene is utilizing Medidata’s unified technology platform to enhance capabilities in data management, study planning and design, trial operations, analytics and patient engagement.
“Celgene’s deep commitment to patients, disruptive science and disease-altering medical innovation is at the heart of their clinical development strategy and, more broadly, the success that they are having in driving medical advances in many of the world’s difficult-to-treat diseases,” said Tarek Sherif, Medidata’s chief executive officer. “We are in the early days of a renaissance in drug discovery, and Medidata’s Clinical Cloud is playing a critical role in helping to power the kind of innovation that will improve the lives of patients around the world.”
Primarily a Medidata Rave® (electronic data capture, management and reporting) customer since 2008, Celgene will expand its use of the Medidata Clinical Cloud to include Medidata Designer® (study and protocol design); Medidata Grants Manager® (site budgeting and planning); Safety Gateway (safety reporting); Medidata CTMS® (clinical trial management); Medidata SQM (site quality management) and Medidata Patient Cloud ePRO (electronic patient-reported outcomes). Celgene is also leveraging one of Medidata’s turnkey clinical analytics offerings, Medidata Insights™, which provides advanced metrics, visualizations and the most powerful set of industry data and benchmarks.
“Drug development is becoming more complex by the day, with researchers exploring vast genomes and proteomes increasing prospects to control or cure disease through precision medicine. Medidata is providing Celgene and a rapidly growing list of other global life sciences companies with an integrated platform and the fundamental analytics and tools needed to optimize drug development programs,” said Glen de Vries, Medidata’s president. “We are thrilled to deepen our relationship with Celgene, a company that shares our passion for pushing the frontiers of science and technology and improving global health.”
About Medidata
Medidata is the leading global provider of cloud-based solutions for clinical research in life sciences, transforming clinical development through its advanced applications and intelligent data analytics. The Medidata Clinical Cloud® brings new levels of productivity and quality to the clinical testing of promising medical treatments, from study design and planning through execution, management and reporting. We are committed to advancing the competitive and scientific goals of global customers, which include over 90% of the top 25 global pharmaceutical companies; innovative biotech, diagnostic and device firms; leading academic medical centers; and contract research organizations.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.