Mission3 Introduces Latest Release of FastCrossing at the 20th Annual Drug Information Agency – Electronic Data Management Conference

Philadelphia, PA – February 9, 2007 – Mission3, Inc., a leading provider of Project and Document Management and e-submission software specifically serving the Life Sciences industry announced today that is has reached a significant milestone in the development of it’s enterprise software suite with the latest release of FastCrossing.

FastCrossing is an electronic submission management application that allows Life Sciences companies to manage their mission critical regulatory submissions, in parallel with their project development, for the FDA as well as European, Canadian, and Japanese counterparts. FastCrossing is a Web-based application that allows for rapid implementation and provides a logical means for controlling specific submission information such as type (NDA, IND, or ANDA) as well as region.

User friendly, FastCrossing assembles and delivers valid eCTD XML and supporting files and folders with the push of a button. It uses a database to store all configurations, making it significantly faster than applications that manage the submission on a file system or in native XML.

"A unique feature of FastCrossing is cloning, the creation of derivative submissions, for regional submissions or new indications. Cloning allows users to select for editing only those parts of a submission that they need to change, allowing the remainder to inherit changes from the original. When coupled with MissionFire's project and document management capabilities, FastCrossing fulfills the requirements of creating an 'Organized Enterprise', ensuring time to market advantage and increasing shareholder value." said Dirk Karsten Beth, President of Mission3.

About Mission3, Inc.
Mission3 was founded to assist biotech, pharmaceutical, and medical device companies to bring needed therapies and devices to market quickly and efficiently. Its advanced enterprise software suite allows companies to manage projects and documents; comply with regulatory requirements; and submit applications in an automated, electronic, and managed environment. Companies taking full advantage of Mission3’s industry leading enterprise software suite can simultaneously create an electronic submission while a project is underway, significantly reducing the time needed to develop a product and submit it for regulatory approval.