Solutions for Pharmaceutical Manufacturers

At Thinspring, we understand that compliance activities do not exist in a vacuum and that gaps in Regulatory Information Management (RIM) can substantially impact your company's core business processes. To help your company meet these challenges ThinSpring solutions combine the best of Structured Content Authoring (SCA) and Software as a Service (SaaS) technology to provide flexible and responsive submissions solutions.

United States Food and Drug Administration (FDA) and Health Canada (HC) - Structured Product Labeling (SPL) and Structured Product Monograph (SPM)

FDA and European Union (EU) Electronic Common Technical Document Submissions (eCTD)

Other Predicate Rule Required FDA Submissions

Other Services

Offering an end to end collaborative service environment for submissions management, ThinSpring delivers a powerful and flexible set of services and tools.