Scottsdale, AZ – Mission3, the Premier Regulatory Information Management provider for the Life Science industry will be exhibiting at the upcoming 2012 RAPS – The Regulatory Convergence Conference. The company will have a booth set up in the exhibit hall (#224) and have team members attending the educational sessions.
The RAPs Annual Conference helps regulatory professionals from around the world and from all aspects of the Life Science industry share knowledge and information so that the safest healthcare products are delivered in an ever changing environment.
“We greatly enjoy being part of the RAPs Annual Conference. The conference is a perfect place to show attendees from the Medical Device community to Pharma and Biotech our DMS, Regulatory, and eTMF solutions. We’ve handled global regulatory information management solutions for Fortune 50 Pharma clients all the way to cloud-based Document Management, electronic Trial Master file, and eCTD Publishing solutions for small to mid sized pharma/biotechs,” said Dirk Beth, President and CEO of Mission3.
“The RAPs Annual conference makes collaborating with other regulatory professionals within the industry easy. I can share my real-world successes in helping companies convert from a paper based TMF process into an electronic Trial Master File. Companies know that they need to move into an electronic process and this conference provides the right venue to educate my colleagues,” said Adair Turner, Regulatory Affairs Manager at Mission3.
Mission3 will be exhibiting at booth #224 during the RAPs Annual Conference.
2012 RAPS – The Regulatory Convergence - Conference
October 26 - 30, 2012
Washington State Convention Center
800 Convention Place
Seattle, WA 98101
Exhibit Booth: #224
Exhibit Hall Hours
Sunday, October 28th: 9:30 am – 6:00 pm
Monday, October 29th: 9:30 am – 3:15 pm
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 and services 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.
