Liquent Regulatory Solutions for Life Sciences |
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May 12, 2008![]() |
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Liquent InSight Suite: Overview Introducing 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, Liquent’s latest generation of solutions, 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.
Unlike legacy systems that are retrofitted with a Web interface, Liquent’s InSight solution is a pure Web solution that address the critical functions of submission management: registrations, projects and lifecycles. Together these solutions help reduce compliance risks and provide maximum revenue opportunity by ensuring products are on track for market approval, and properly maintained over the life of the product, all through a configurable Web interface.
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