Sanofi Selects Medidata Clinical Cloud as a Technology Standard Across Global R&D Organization

Top 5 Pharma Chooses Medidata Platform for Cutting-Edge Productivity, Cost Savings and SaaS Ease-of-Use to Benefit Multiple Trial Areas

Sanofi Selects Medidata Clinical Cloud as a Technology Standard Across Global R&D Organization

<0> Medidata SolutionsLineene Krasnow, 212-918-1761 </0>

(NASDAQ: MDSO) has been selected by Sanofi, one of the world’s leading pharmaceutical companies, as the clinical technology standard for clinical data collection, management and reporting and performance-enhancing analytics across its entire R&D organization. Sanofi is actively transitioning to replace some of its existing clinical technologies with Medidata’s cloud-based solutions across all Sanofi Global R&D as part of a company-wide initiative to achieve cutting-edge productivity.

Sanofi manages one of the largest R&D organizations in the industry, with a diverse pipeline in vaccines, diabetes, oncology and orphan drugs, among other areas. Sanofi is focusing on maximizing the efficiency of its clinical development organization as well as improving visibility into the progress of its global trials, and undertook a competitive evaluation of clinical technology to support its research goals.

Sanofi will implement Medidata’s electronic data capture, management and reporting, coding and safety data capture applications. Additionally, the organization chose Medidata’s clinical business analytics tool to provide metrics and industry benchmarks that enhances decision-making by executives and operational managers throughout the trial life cycle.

Implementation of Medidata’s cloud-based platform will enable Sanofi to achieve a range of new benefits throughout the trial process and through a single URL globally:

is a leading global provider of cloud-based clinical development solutions that enhance the efficiency of customers’ clinical trials. Medidata’s advanced platform lowers the total cost of clinical development by optimizing clinical trials from concept to conclusion: from study and protocol design, trial planning and budgeting, site negotiation, clinical portal, trial management, randomization and trial supply management, clinical data capture and management, safety events capture, medical coding to business analytics. Our diverse life science customer base spans biopharmaceutical companies, medical device and diagnostic companies, academic and government institutions, CROs and other research organizations, and includes more than 20 of the top 25 global pharmaceutical companies as well as organizations of all sizes developing life-enhancing medical treatments and diagnostics.

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