Virtify SPL global labeling solution is designed for organizations to meet the SPL and PLR standards put forth by the U.S Food and Drug Administration (FDA). Companies can use Virtify SPL to author, publish, review, and save SPL-compliant labels. Conversion of legacy labels created using Microsoft® Word is built into the system.
- Ajax enabled
- Categorize labels by Product, Country and Submission Type
- Create Label Templates
- Create Labels based on an existing template
- Import XML labels
- Track and retrieve current, proposed and approved versions of a label
- Support for SetID and rootID Life Cycle Management
- Render in various formats
- SPL XML
- SPL XML with FDA standard Style sheet
- Rich Text Format (RTF) for viewing in Microsoft Word Format
- Portable Document Format (PDF)
- Track Document and Section Level Versions
- Revert to an existing version
- Create and Manage Library Content
- Clone Content from Library for use in multiple labels
Virtify SPL's inbuilt artificial intelligence capability highlights any deviance from the FDA SPL schema at the time of authoring, eliminating the need to spend effort downstream. Since Tier 1 and Tier 2 validation takes place against the xsd schema put forth by the FDA, a label created by Virtify SPL is guaranteed to be accepted by the FDA.