Thomson Reuters

As industry and regulatory authorities look to unify the submission structures through the CTD and eCTD, Life Sciences organizations are looking for integrated solutions that can effectively manage product registrations, dossiers and documents over time.

Liquent InSight  is the first and only product suite to provide a centralized, global view of product details, documents, and submissions to support collaboration, compliance requirements and the eCTD.

• Submission materials via product and application information
• The ability to effectively manage the entire regulatory information lifecycle
• Internal resources to focus on core competencies
• Traditional paper CTDs and hybrids
• Over 300 paper CTDs in the US

Each of the three components of Liquent InSight can work independently, but are much more beneficial when integrated and deployed across your enterprise. Together, they support the entire regulatory product management lifecycle.

Liquent InSight includes:

• Liquent InSight Manager - Supports the entire regulatory product management lifecycle, from the early planning of registration targets through to product retirement.
• Liquent InSight Publisher - Quickly and easily create, review, amend and submit regulatory dossiers
  
• Liquent InSight Viewer - Viewing, reviewing and collaboration capabilities for in-process and submitted eCTD materials.