Clinovo Launches New CDISC Express Service Packages

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Using CDISC standards to run faster, efficient clinical trials.

CDISC Express is the only CDISC SDTM conversion tool that maps all your clinical data in just one click

Clinovo, the leading clinical data solution provider in the San Francisco Bay Area, announced today the launch of three CDISC Express service packages, adapted to different needs and different budgets. The offer helps pharmaceutical, biotechnology and medical device companies streamline their clinical trials process by using CDSIC SDTM standards.

Following requests from the user community, Clinovo introduced three different CDISC Express service packages. The services include clinical data conversion to CDISC SDTM, CDISC Express training and validation, and a responsive online helpdesk. Leveraging years of experience and know-how in CDISC conversion, Clinovo is able to quickly and easily map clinical data to the FDA recognized CDISC standard.

Clinovo’s service offering have been specifically packaged to fit the different needs of life science companies. By using their in-house free SAS-based mapping tool CDISC Express, the service packages defeat all prices on the market. All the service packages come with full service CDISC help desk support and study mapping to CDISC SDTM. The Pro package also comes with hands-on training of CDISC conversion, while the Enterprise package provides a validation kit for CDISC Express.

Clinovo has been freely distributing CDISC Express, a SAS®-based application that automatically converts clinical data into CDISC SDTM. CDISC Express was designed by Clinovo to facilitate and accelerate FDA review, thus enabling pharmaceutical, biotechnology and medical device companies to deliver their medical innovations faster to patients.

Since its launch in May 2011 at the annual PharmaSUG Conference held in Nashville Tennessee, over 400 industry professionals downloaded the application. “CDISC Express is the only CDISC SDTM conversion tool that maps all your clinical data in just one click”, explains Jiangtang Hu, SAS programmer at Sanofi-Aventis.

Complying with CDISC standards is a way to streamline the clinical trial process. As the standard format recommended by the FDA for clinical trial data submission, using CDISC standards:
-- Facilitates the FDA review process
-- Improves efficiency for clinical data exchange
-- Ultimately reduces costs and speeds up time to market

Clinovo is committed to improve the clinical trials process by helping expand the adoption of CDISC standards. As a CDISC Gold member, Clinovo is actively promoting CDISC, a non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. Clinovo regularly organizes free webinars and events on CDISC standards.

About Clinovo
You Innovate. We Accelerate. TM
Clinovo is the phase I clinical trials expert in the San Francisco Bay Area. Clinovo’s commitment: Accelerate early phases clinical trials. Leveraging years of industry and technology expertise, Clinovo delivers top-end clinical trial services that enable life sciences companies to bring their medical innovations faster to market. Clinovo’s range of services includes:Clinical Data Management, Electronic Data Capture, CDISC mapping and SAS Programming.

Contact information
Sophie McCallum, Marketing Manager
Email: sophie(dot)mccallum(at)clinovo(dot)com
Phone: 408-773-62


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Sophie McCallum
+1 (408) 773-6258
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