South San Francisco Based BioScience Company Implements Mission3 OnDemand

March 29, 2011 - PRLog -- With a primary focus on development of therapeutics for Alzheimer’s and Parkinson’s disease, the company will utilize Mission3 OnDemand to manage their development efforts and support their regulatory operations. Mission3 OnDemand will provide a collaboration platform for their worldwide development team to manage their critical development and business documents.

The company chose Mission3 as their technology vendor of choice for 3 primary reasons: ease of use, breadth of capability and the Software-as-a-Service (SaaS) delivery model. The ease of use stems from the fact that solution is designed for Life Sciences business users in mind. Further since it is 100% web-based it can be instantly rolled out to both internal as well as external partners in a highly secure manner. Mission3 OnDemand offers Submissions Publishing integrated with Document Management, so all regulatory content needs of the company’s regulatory content can be provided via a single platform that is 21 CFR Part 11 compliant. Last but not least, the SaaS architecture protects the company from high initial IT infrastructure costs. The solution provides them with a highly secure and scalable IT environment with no hardware investments and financed via a “pay-as-you-go” pricing model for the software. The resulting cost benefits are critical for the company, which is in its early stages of evolution.    

“This is an exciting opportunity for Mission3.  Our technology platform seamlessly integrates critical technology components such as Document Management, Virtual Data Rooms, and Regulatory Submission Publishing, for Life Science companies.  Instead of creating silos, we create efficiency and business value. Mission3 OnDemand allows emerging companies to focus on their development work while leaving the IT side of the business to us”, said Dirk Karsten Beth, CEO of Mission3, Inc.

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.

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Mission3 is a provider of SaaS software that merges technology with affordability, exclusively for the Life Sciences industry. Mission3 OnDemand is a fully integrated Document, Project, Regulatory Submission Management and virtual data room suite.