Phoenix, AZ – February 23, 2011 – Mission3, Inc., the premier Regulatory Information Management software company for the Life Sciences industry announced today that Pharma Consulting Solutions has selected Mission3 OnDemand to fulfill its regulatory submission management needs.
Pharma Consulting Solutions (PCS) specializes in helping clients develop and execute their worldwide regulatory submission management strategy. PCS has extensive experience with therapeutics, Over-The-Counter, and medical device development with particular specialties in ophthalmic pharmaceuticals and dietary supplements.
Mission3 OnDemand is a web-based platform that provides Life Science companies with the collaboration tools necessary for transforming their compounds or devices from proof of concepts to commercialization or strategic partnerships. Mission3’s tools and capabilities include Document Management, Global Regulatory Submission Management and Tracking, Project Management, Virtual Data Room, and Collaborative Authoring – all of which are tightly integrated to maximize productivity and ultimately shorten the time to market.
“Finding a document management suite for a consulting and contracting company whose members are spread across North America was no easy feat for PCS. We wanted a solution that was 21 CFR Part 11 compliant, deployed as Software-as-a-Service with an easy to use dashboard. Additionally we wanted a provider that delivered strong customer service. We chose Mission3 based on the integrated document and submission management tools, and the fact that we did not have to incur any IT expense. We were able to be up and running within a month and will be pushing out an NDA submission in the next three months.” said Susan Augello-Vaisey, Managing Partner, Pharma Consulting Solutions.
“Mission3 is helping PCS implement a strategy of working smarter so that they can provide their customers with increased value and insight into their product development and corresponding regulatory submissions. We designed Mission3 OnDemand for companies like PCS so they can fulfill client commitments swiftly, without having to plan out a long implementation period or make huge IT investments. After all, they are in the regulatory information management business, not the IT business”, 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.
CONTACT INFORMATION:
Chris Joslin Chief Operating Officer Mission3, Inc. www.mission3.com 602-957-2150 cjoslin@mission3.com
