Understand The Regulatory Environment
Speed Access to Product Information
Regulatory professionals are challenged daily with
gathering data and information from a variety of sources
in order to stay on top of submission schedules and internal
reporting
demands. Information about the medical products in stored
in a variety of disparate hard copy files and network
databases that are not well linked.
Structured content management holds the promise of tying
this information together throughout the products entire life
cycle. Today, however, in the realm of medical product
regulatory operations that promise is tied up in an alphabet
soup of standards and committee acronyms, XML, SPL, RCRIM,
eCTD, PIM, CDISC, GEML amongst others.
ThinSpring solutions offer regulatory professionals
an evolutionary path towards realizing the promise of structured
content management. Native format editing tools allow
you to create and manage structured content without having
to learn how to be a computer programmer. Easy to use reporting
tools and email notifications help you stay on top of multiple
deadlines and management requests.
One size does not fit all for the medical products manufacturing
industries. A company that is currently marketing
only a few medical products in the United States has much different
needs then one marketing hundreds on a world-wide basis. Our
team's flexible set of outsourced services and web based tools
help you choose the solution that fits your needs best.
To find out how our products can help you harness the
power of structured data, check out SPL Server. If
you want to learn about other options that are built into our
structured data management solutions, read the XML Sage product
information.
Copyright © 1996-2007 by ThinSpring.
All Rights Reserved. | Legal Info
MojoCommerce LLC is doing business as ThinSpring.