The only browser-based fully integrated document management, assembly, publishing and product registration tracking suite
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. Clearly, recognizing and understanding the impact of new regulations is vastly important to positioning your organization for successful product development, launch and maintenance.
The Liquent InSight® Suite 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.
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Liquent InSight Suite includes the following products:
Liquent InSight® Manager — supports the entire regulatory product management lifecycle, from the early planning of registration targets through to product retirement
Liquent InSight® Publisher — enables you to quickly and easily create, review, and amend regulatory dossiers, and submit them for market approval.
Liquent InSight® Viewer — provides viewing, reviewing and collaboration capabilities for in-process and submitted eCTD materials.
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