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.
Products in this suite
-
Liquent InSight Manager
Tools to help your global coordination of regulatory project planning, product detail management, and dossier creation.
-
Liquent InSight Publisher
Software and submission templates to simplify and speed up the creation and review of regulatory dossiers.
-
Liquent InSight Viewer
Unique, secure regulatory submissions viewer supporting the sharing and collaboration of eCTD files.
Contact Us
North America:
Tel: + 1 215.328.4444
Europe:
Germany & Eastern Europe
Tel: +49 89.547.56.180
UK & Northern Europe
Tel: +44 2074.334000
France, Benelux & Southern Europe
Tel: +33 1.53.06.20.00
Asia:
Tel: +81 3.5218.6505
Next Steps
- Regulatory Software & Related Services
- More Pharmaceutical & Biotechnology Solutions
- Factsheet PDF
- Product Inquiries
Already a Customer?
- Liquent Customer Lounge : Open to all Liquent InSight, CoreDossier, EZsubs and PDFaqua users. The Liquent Customer Lounge enables you secure, real-time access to the information you need.
- Technical support
- Training