PhRMA Trade Association Selects Medidata Solutions’ Extensive Real-world Cost Databases for Clinical Trial Analysis

Leading Pharma Industry Association and Economic Consulting Firm Leverage Medidata’s Extensive Proprietary Databases to Assess Post-approval Clinical Studies

PhRMA Trade Association Selects Medidata Solutions’ Extensive Real-world Cost Databases for Clinical Trial Analysis

<0> Lois Paul and PartnersSusan McCarron, 617-986-5767 </0>

The major trade group for the global pharmaceutical industry, (PhRMA), and economic consulting firm (AG) have selected benchmark industry tools from (NASDAQ: MDSO) as the key input for research into the costs of post-approval clinical trials.

Clinical trials are one of the costliest areas in bringing safe and effective new treatments to patients. After a medicine has been approved for initial use, pharmaceutical companies often invest further in determining its effectiveness and safety for new populations, such as pediatric patients. PhRMA and AG are analyzing the costs associated with these post-approval trials, identifying cost drivers and variations.

The research will rely on the world’s largest databases of negotiated clinical costs from and , which have the PICAS and CROCAS databases containing hundreds of thousands of data points from actual executed protocols, investigator grants and other contracts from pharmaceutical and other research sponsors.

Working with AG, a widely-recognized group of health economics experts, PhRMA will deliver the key data points that will form the foundation of this research.

Medidata Grants Manager and Medidata CRO Contractor are widely used by pharmaceutical companies, medical device companies and contract research organizations to conduct fair and efficient trial planning, budget development and grant negotiation. Considered the industry standard for measuring trial cost trends, these globally accessible analytic tools have also been used for research by the National Bureau of Economic Research and other research organizations.

(PhRMA) represents the country’s leading pharmaceutical research and biotechnology companies, which are devoted to inventing medicines that allow patients to live longer, healthier, and more productive lives. PhRMA companies are leading the way in the search for new cures. PhRMA members alone invested an estimated $49.5 billion in 2011 in discovering and developing new medicines. PhRMA's mission is to conduct effective advocacy for public policies that encourage discovery of important new medicines for patients by biopharmaceutical research companies.

provides a broad range of economic, financial, management and litigation support consulting to corporations, government agencies, and law firms, and is a leading provider to life sciences firms of health economic analyses and outcomes research. The firm, founded in 1981, has over 500 professionals, with offices in Boston, Chicago, Dallas, Denver, Los Angeles, Menlo Park, New York, San Francisco, Washington, and Montreal.

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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