Meet Mission3 in the EDM & eSubmission Pavilion at Drug Information Association Annual Meeting
6/12/2013 2:24:27 PM
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Phoenix, AZ – Mission3, the Premier Regulatory Information Management provider for the Life Science industry will be exhibiting in the EDM & eSubmission Pavilion (Booth #1010) at the DIA Annual Meeting June 24-26 in Boston.
Mission3 was the first solutions provider to offer the Life Science industry a cloud based solution for Regulatory Information Management - Clireo. Clireo is designed to easily meet several specific needs of Life Science companies, such as Electronic Trial Master File (eTMF), Electronic Document Management System (eDMS), Submission Management, and Electronic Management of Promotional Materials (eMPM).
“I think its great to see more and more companies moving to the Cloud. This just further validates the plan Mission3 developed years ago to provide key regulatory information management systems to Life Science companies in an on-demand environment. The companies are in the drug development business, not the IT business and shouldn’t invest scarce capital and resources building applications and data centers from the ground up,” said Dirk Karsten Beth, CEO of Mission3.
Recognizing the adoption of SharePoint by Life Science companies and their need to take advantage of the investment in that platform, Mission3 also developed GlobalTrack. GlobalTrack is an enterprise solution for Regulatory Information Management that encapsulates planning, tracking, correspondence management, and xEVMPD (soon IDMP). GlobalTrack easily integrates with existing life-of business applications and provides increased visibility into global regulatory initiatives.
Mission3 will be exhibiting its solutions at Booth #1010.
DIA Annual Meeting
June 24th – 26th, 2013
Hynes Convention Center
Exhibit Booth: #1010
About Mission3, Inc.
Mission3 is the premier Regulatory Information Management Software Company for the Life Sciences industry. Mission3’s solution includes electronic document management solutions for managing regulatory, clinical and corporate documents; Virtual Data Rooms to securely manage the due-diligence process for M&A and partnerships; full regulatory submission management that includes support for eCTD, 510(k), PMA, as well as paper and electronic publishing to compliment submission and dossier management. Topping off this extensive list of solutions to the Life Science industry is Mission3 GlobalTrack, a business intelligence platform that provides companies increased visibility into their global regulatory initiatives. All Mission3 solutions are 21 CFR Part 11 compliant.
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