GlobalSubmit 2010 Now Available: Expands Product Suite with New PUBLISH™ and CROSSCHECK™ Functionality

PHILADELPHIA, Jan. 19, 2011 /PRNewswire/ -- GlobalSubmit Inc., (www.globalsubmit.com) a leading developer of software designed exclusively to publish, validate and review electronic Common Technical Document (eCTD) global submissions, announces the release of GlobalSubmit 2010. This latest version introduces all-new PUBLISH™ and CROSSCHECK™ functionality, along with several new features in its flagship products, VALIDATE™ and REVIEW™, designed to enhance performance and usability, facilitate successful submissions and keep clients in accordance with the FDA.

PUBLISH is an end-to-end solution for assembling, validating and publishing regulatory submissions that allows users to easily build their application as the FDA sees it. CROSSCHECK is a quality assurance module that cuts days off the time it takes to quality check bookmarks and hyperlinks, ensuring timely, accurate submissions.

Additional highlights include:

VALIDATE

• PDF Files/Error Checks - over 30 newly added error checks of PDF files to avoid costly errors that can lead to technical rejection.
• Additional Formats and Regional Support - includes eCTD support for EU, Health Canada, SwissMedic and TGA as well as support of NeeS and RPS standards.

REVIEW

• Origin View - addresses the file ordering issues that arise from lifecycle management by maintaining a view of submissions in the original order for the FDA to see.
• Data Management - enhanced organization of sections, including lifecycle file ordering, inclusion of orphaned files folder, updates to viewing Study Tagging Files (STFs) and more.

GlobalSubmit's CEO Rahul Mistry says, "Our goal with GlobalSubmit 2010 is to enable clients to create high quality submissions quickly and simply. The addition of PUBLISH and CROSSCHECK rounds out our product suite, while also saving clients more time than ever before and assuring quality eCTD submissions. The recent upgrades are a direct result of collaborative user feedback and continued leverage of our extensive, firsthand knowledge of FDA requirements. I am excited to announce this latest release, and look forward to the continual advancement of GlobalSubmit."

GlobalSubmit 2010 will be showcased at the 24th Annual DIA Electronic Document Management Conference on February 15-16, 2011.  Visit the GlobalSubmit booth #401, or contact GlobalSubmit to learn more.

About GlobalSubmit

GlobalSubmit is a products and services company that provides transparency in regulated healthcare products. The U.S. Food & Drug Administration and leading Life Sciences companies use our flagship software applications, REVIEW™ and VALIDATE™, to review and validate electronic submissions. GlobalSubmit's thought leaders lead international efforts, constantly working with the industry and with government agencies to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.

SOURCE GlobalSubmit Inc.