How to reduce risk while increasing speed with labelling structured content
Learn how to simplify content processes and reduce risk by standardizing and centralizing the content collation process
Reduce risk by using a technology platform that standardizes the content collation process, defines content ownership, promotes content reuse, and tracks changes for IFUs, leaflets, artworks and other documents for submission to regulatory bodies
This webinar will explore best practice solutions to help improve the labelling process for life sciences companies by managing and simplifying the content process.
Structured content management software can enable pharma companies to create, approve, translate and transfer content from a single tool. It can also help companies to update content faster with impact reports to assess and initiative change, improve version control and automatically create and send Word documents and InDesign leaflets based on approved content.
This panel session will provide insights into how a major pharma company has adopted content management and how to address change management, migration and other considerations for implementing a content management solution.
Register for this webinar to learn:
- The challenges associated with managing content, including labelling, packaging, artwork, IFUs and more
- How to use technology to manage structured content and easily make updates to content for regulatory submission
- The considerations to make before implementing a content management software, including change management and migration
- The benefits content management solutions can bring to your company
Speakers
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