Meeting your regulatory publishing needs
Liquent EZsubs offers a full range of publishing capabilities seamlessly integrated into the Documentum® user interface. These enable you to meet your regulatory publishing needs, thus helping you achieve quality, accuracy, and data integrity to deliver regulatory reports and submissions reliably and on time. It is an industry-proven solution, suitable for all sizes of pharmaceutical, biotech and CRO organizations that are required to create compliant electronic and paper submissions.
Whether you are in the early stages of drug development or submitting a full scale dossier, EZsubs provides the ability to accelerate each stage of your product development lifecycle. It also provides a fully localized option for Japanese submissions and Japanese operating systems. EZsubs assures alignment with the latest regulatory guidance’s, providing a solution for submissions to worldwide regulatory agencies, with submission templates for quick and easy assembly including CTD/eCTD templates.
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- Streamlined and seamless eCTD publishing
- Compile simultaneous submissions to global agencies achieved by comprehensive built-in templates
- Volumize large paper-based submissions
- Resolve electronic cross references between documents and volumes for electronic submissions
- Conserve resources with support for individual users with “roles based” interfaces
- Network optimization tools for globally distributed teams on corporate networks
- Transform file formats to PDF while maintaining full page fidelity
- Achieve site driven load balancing for rapid performance
- Operate with low footprint and low load on the corporate IT systems
- Achieve faster installation and deployment then any other software on the market
- Utilize the Unicode base for complete Japanese submissions
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EZsubs provides an effective and highly reliable publishing tool to support your organization during mission critical submission periods:
- Seamlessly transition prior submissions to new eCTD format
- Faster time to submission with automated publishing process: quickly assemble an eCTD from scratch
- Increased productivity with powerful tools for fast resolution of electronic cross references between documents and volumes for electronic submissions
- Assured compliance with the latest regulatory guidelines and specifications
- Simultaneous submissions to multiple agencies achieved by comprehensive built-in templates
- A single solution to compile compliant submissions in both electronic and paper format. Reduced resource requirement for submission preparation with automated tools to support paper publishing
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