Medidata Solutions Partners with Veeva Systems to Bring Integrated eTMF to the Clinical Cloud

Cloud Technology Integration Gives Sponsors Path to Faster Regulatory Submissions

Medidata Solutions Partners with Veeva Systems to Bring Integrated eTMF to the Clinical Cloud

<0> EdelmanGeoff Curtis, 312.233.1253orVeeva Systems, Inc.Lisa Barbadora, 610.420.3413 </0>

has partnered with (NASDAQ: MDSO) to offer the life science industry’s first cloud-based end-to-end solution that integrates clinical documentation and trial development. The two companies will integrate , Veeva’s electronic trial master file (eTMF) content management application, across the , offering life science companies and their global partners a complete clinical technology solution with a searchable central repository for all clinical documentation.

As clinical trials become more and more complex, the need for dependable document storage combined with real-time data accessibility is vital. The partnership will meet this need, advancing technology platform offerings in clinical development by facilitating efficient management of the trial master file collection. The integrated solution also provides secure document exchange between sites and sponsors, reducing the need for separate enterprise collaboration systems and portals. The collaborative nature of the clinical research team also demands a solution that is globally accessible and meets both regulatory and security needs.

is a cloud-based solution that provides clinical trial sponsors and contract research organizations (CROs) with real-time access to clinical documentation throughout the clinical trial process. Integrating Vault eTMF with Medidata’s suite of solutions, including electronic data capture (EDC), clinical trial management system (CTMS) and risk-based monitoring, saves valuable IT implementation time and costs by eliminating the need for multiple integrations of eTMFs and clinical systems across a trial’s processes. Additionally, the partnership will speed trial start-up, reduce compliance risk and provide better visibility into trial processes.

is the leader in cloud-based business solutions for the global life sciences industry. Committed to innovation, product excellence and customer success, Veeva has over 150 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Founded in 2007, Veeva is a privately held company headquartered in the San Francisco Bay Area, with offices in Philadelphia, Barcelona, Budapest, Paris, Beijing, Shanghai and Tokyo.

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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