Phoenix, AZ – February 1, 2010 – Mission3, Inc., a leading Regulatory Information Management provider for the Life Sciences industry, will be exhibiting at the DIA Electronic Data Management Conference next week in National Harbor, Maryland. In addition, Dirk Beth, the President and CEO of Mission3, will be hosting a panel session on “Management of Product Registrations in a Global Regulatory Environment”.
Dirk will discuss key areas that Life Science companies must contemplate when developing their global submission strategy - internal planning, business intelligence gathering, and regulatory information management.
“I am excited to provide the latest thinking on Regulatory Information Management during the panel discussion at the conference. Based on its extensive experience with Life Science companies, Mission3 has unique insights to share on the topic, specifically in the area of regulatory intelligence and submissions management. I’m honored to be part of the thought leadership and expertise that the DIA has pulled together for the conference attendees and thrilled to have the opportunity to speak at this event”, said Dirk.
Please put this event on your calendar and join us. The DIA Electronic Data Management Conference will provide attendees with an interactive opportunity to design and develop business processes to convert your companies’ mountains of data into appropriate document components that will be used in all your regulatory submissions. The EDM Conference will also focus on managing information in a completely electronic environment, while enabling your organization to meet the current and future electronic submission standards.
DIA Electronic Data Management Conference February 15-17, 2011 Gaylord National Hotel and Convention Center 201 Waterfront Street National Harbor, MD 20745 Mission3: Booth #305 http://www.diahome.org/
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 Operations Officer Mission3, Inc. www.mission3.com 602-957-2150 cjoslin@mission3.com
