Mission3 Leads Discussion At The Global Clinical Outsourcing Summit Conference

Mission3, the premier Regulatory Information Management software provider for the Life Sciences industry will lead two panel sessions at the Global Clinical Outsourcing Summit Conference this week at the Sheraton Meadowlands in East Rutherford, NJ.

This executive-level event will focus on the unique issues involved in outsourcing clinical research and life sciences manufacturing to non-US locales; and on the regulatory, logistical and technology-related issues that are empowering global partnerships.

Dirk Beth, CEO of Mission3, and Adair Turner, Regulatory Affairs Manager, will lead a panel on “Moving into the Fast Lane with eTMF” that will discuss using electronic Trial Master Files from a multitude of perspectives – business, regulatory affairs, and customers.

Additionally, Dirk will also be speaking on another panel “Managing Relationships in Over 10, 20 or More Countries”. Pharmaceutical and biotechnology companies are increasingly expanding their market opportunities for new products by applying for regulatory approvals in multiple countries simultaneously rather than sequentially.

Additionally, Mission3 will be exhibiting its Regulatory Information Management solutions for Life Science companies at the conference.

What can be done by sponsors; CROs and clinical research; and manufacturing sites to drive innovation with continually limited resources and budgets? As Sponsors reduce internal resources, dependence on outsourced relationships with partners, consultants, and CROs have continued to increase. Outsourcing and strategic partnerships have never been more imperative to unlocking value, driving down costs, and reducing drug delivery time. Many believe that contract research organizations with a global presence will continue to benefit from these trends.

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 GlobalTMF. All Mission3 solutions are 21 CFR Part 11 compliant.

SOURCE: Mission3, Inc.