As you know, industry and regulatory authorities have been unifying registration and submission processes. In fact, with the CTD and eCTD, submission activities are now more integrated than ever before. That means finding an integrated solution is all the more critical.

With Liquent InSight® from Thomson Reuters, you will have a centralized view of all the moving parts, including product details, change control, tracking, documents, and submissions to support change control, tracking and compliance requirements for the eCTD as well as other submission formats. As a result, you’ll be able to more effectively manage product registrations, dossiers and documents over time, as well as crucial operational systems.

So, why not bring it all together? With Liquent InSight, you can support the entire regulatory lifecycle.

You'll be able to

 Utilize efficient and compliant change control tracking of product detail, data and submission documents

• Access a regulatory focused data library and reporting framework
• Locate publishing support for eCTD, paper, hybrid, NeEs, medical device (PMA/510k), and others
• More effectively manage the entire regulatory information lifecycle