NEW YORK--(BUSINESS WIRE)--Medidata Solutions (NASDAQ: MDSO), a leading global provider of SaaS-based clinical development solutions, today announced its latest services offering, Medidata Standards Accelerator^TM, which provides end-to-end support for the Clinical Data Interchange Standards Consortium (CDISC) study data tabulation model (SDTM) – the FDA’s recommended format for electronic submission of case report form data. With this offering, Medidata enables sponsors to satisfy FDA submission guidelines in a repeatable fashion, while reducing time and costs.

Medidata’s experienced services team works with sponsors using the Medidata Rave® electronic data capture (EDC) and clinical data management (CDM) platform throughout the study lifecycle to streamline the preparation of SDTM-ready data and the export of SDTM-compliant datasets. In addition to the best practices utilized by Medidata services professionals, Standards Accelerator includes multiple tools aimed at streamlining the preparation of SDTM-compliant data sets:

• Pre-built CDASH forms for 17 standard SDTM domains;
• Rave dictionaries using CDISC-controlled terminology;
• Edit checks for SDTM validation rules to minimize data errors.

A longtime CDISC Corporate Sponsor and Registered Solution Provider, Medidata has had a number of its executives formally recognized by CDISC for their individual contributions to standard definitions and ongoing participation in standard groups. Additionally, Rave was the first to be software product certified on all eight Operational Data Model (ODM) use-cases for full interoperability and sharing of clinical data. Rave also was the first EDC solution to provide clinical data acquisition standards harmonization (CDASH) metadata. Medidata Designer®, a study protocol and design solution, has contributed its model to CDISC’s protocol representation model.

“Medidata Standards Accelerator builds on our continued commitment to true interoperability across clinical systems by leveraging CDISC standards,” said Glen de Vries, president of Medidata Solutions. “From ODM to SDTM and others, we will continue to incorporate leading standards across the development process in our platform capabilities and service offerings.”

About Medidata Solutions Worldwide

Medidata Solutions is a leading global provider of SaaS clinical development solutions that enhance the efficiency of customers’ clinical trials. Medidata’s advanced solutions lower the total cost of clinical development by optimizing clinical trials from concept to conclusion: from study and protocol design (Medidata Designer^®), trial planning and budgeting (Medidata Grants Manager^®, Medidata CRO Contractor^®), site negotiation (Medidata Grants Manager Contracting™), clinical portal (iMedidata™), randomization and trial supply management (Medidata Balance™), clinical data capture and management (Medidata Rave^®), monitoring (Medidata Rave Monitor, Medidata Rave Targeted SDV), safety events capture (Medidata Rave Safety Gateway), medical coding (Medidata Coder™) to business analytics (Medidata Insights™). 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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