Understand The Regulatory Environment

Speed Access to Product Regulatory 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 is 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. In the realm of medical product regulatory operations that promise is defined in an alphabet soup of standards and committee acronyms, XML, SPL, RCRIM, eCTD, XEVPRM, IDMP, 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 edit 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.