Phoenix, AZ – August 18, 2011 – Mission3, the premier Regulatory Information Management software provider for the Life Sciences industry, announces that a biotech client will utilize the Mission3 OnDemand Virtual Data Room.
Mission3’s Virtual Data Room (VDR) helps companies accomplish due diligence by providing a secure content viewer along with robust reporting and tracking capabilities. Mission3’s VDR include a, complete document support, compliant audit trial, rich reporting, document watermarks and time stamps, CAD file support, search capabilities, custom rights management and multi-platform support.
“We are pleased to bring on another life science company who realizes that their Virtual Data Room should be easy to use, efficient, Part 11 compliant and have a robust back-end functionality. Nautilus is a group of enlightened life science leaders and it shows in their decisions”, said Dirk Karsten Beth, CEO of Mission3.
"We needed a Virtual Data Room to support our business development needs and wanted a company with strong experience in the Life Sciences Industry. We were looking for a VDR that was efficient and easy to use. Mission3 was the logical choice because of their versatile products, knowledge, and experience", said Neil Milano, CFO of Nautilus Neuroscience.
Nautilus Neuroscience is a new name to pharmaceutical business, but the people are veterans of the industry. Nautilus is not part of “big pharma” and that is by design. The small size allows them to be responsive and have intimate engagement with customers. Yet it doesn’t prevent them from delivering results for patients, neurologists and other physicians, nurses, investors and all their constituents. Their goal is to develop products, and keep the value of products in the field of neurology for the benefit of all.
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.
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