Regulatory solutions that drive innovation

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A centralized, global view of regulatory documents and submissions

As industry and regulatory authorities unify their submission structures through the Common Technical Document (CTD) and the electronic Common Technical Document (eCTD), life sciences organizations need an integrated solution that enables them to manage product registrations, dossiers and documents effectively over time.

Recognizing and understanding the impact of new regulations is vital to positioning your organization for successful product development, launch and maintenance.

Liquent InSight®, the latest generation of solutions from Liquent, a Thomson business, provides a centralized, global view of product details, documents, and submissions to support collaboration, compliance requirements and the eCTD.

Together, these solutions help reduce compliance risks and provide maximum revenue opportunities by ensuring that products are on-track for market approval, and properly maintained over their lifecycle.

Each of the three components of the Liquent InSight suite — Liquent InSight Manager, Liquent InSight Publisher and Liquent InSight Viewer — can work independently, but are much more beneficial when integrated and deployed across your enterprise.

Together, they support the entire regulatory product management lifecycle from the early planning of registration targets through to product retirement.

Further information

Click here to download the Liquent InSight^® fact sheet