Mission3 Educates At The DIA Regulatory Information Management Conference

April 23, 2012 - PRLog -- Regulatory departments are continually being asked to do more with less. In addition, regulatory authorities are increasing the scrutiny related to patient safety and compliance with approved application information. As regulatory departments are challenged to develop global regulatory strategies, coupled with the corporate desire to launch in global markets early, the need to understand the regulatory requirements for filing, timelines, as well as which products are approved in multiple markets is becoming a critical regulatory need for both industry and regulators.

“GlobalTrack is the only first fully integrated Microsoft SharePoint Regulatory Information Management solution for Life Sciences. GlobalTrack significantly increases companies’ quality and efficiency due to the integration of data from existing line-of-business systems. GlobalTrack extends Project Server for regulatory and clinical activity and document planning. Using Project Server allows companies to leverage Mission3’s comprehensive features plus Project Server’s best-in-class project management features such as resource and financial planning,” says Mission3’s President and CEO Dirk Beth.

Mission3 has created GlobalTrack RIM Solution so that Life Science companies could meet these regulatory challenges. GlobalTrack is the only SharePoint and Project Server based system providing truly comprehensive, integrated and platform-based solution for Regulatory Operation and Planning teams. GlobalTrack focuses on integration of data from the source system of truth to increase efficiency, quality, and compliance. Multiple system integration allows companies to utilize funds where needed most while accomplishing their goals and meeting deadlines.

Mission3, Microsoft, and NNIT are holding an exclusive event Illuminate Your Regulatory World on April 23, 2012 at 4:00pm at the Microsoft Technology Center in Malvern, PA.  Join colleagues and industry experts on the path forward in Regulatory Information Management.  Topics will include the future of regulatory planning, tracking, submissions management, health authority correspondence management, and xEVMPD. Additional discussion will center on the advantages of platform-based solutions and the benefits of integrated solutions.

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 increase visibility into their global regulatory initiatives.  All Mission3 solutions are 21 CFR Part 11 compliant.  Mission3 is a Microsoft Gold ISV Partner.