Veeva PromoMats
Medical, Legal, and
Regulatory Review
Fastest path to approved content.
Building the Future of MLR with AI: Fastest Path to Approved Content
Overview
Industry-specific MLR solution
Tier-Based Review
A variable approach informed by content reuse, reducing average time to approval by 50-75%.
eCTD Compliance Package
Generate submission-ready forms, decreasing manual efforts through automation.
Redline Annotations
Automatically redline annotate references reducing manual effort and eliminating delays due to improper annotations and redline formatting for FDA submission.
Automated Review Workflows
Ensure global consistency while supporting local regulatory needs.
Content Similarity
Drives faster time to market with similarity score calculations.
Multi-document Workflows
Submit several documents for a campaign out at once, whether to author, review or approve.
Impact
Driving Efficiencies with MLR
57%
reduction in review cycle times
55%
reduction in time spent in MLR/PRC meetings
25%
reduction in time spent on compliance procedures
Why Veeva PromoMats
Achieve a faster time to approve content using Content Similarity and Tier-Based Review.
“The ability to bring everybody together and have the MLR review automated, and the digital content stored on one single repository, and to be able to push it out in a common way… that’s amazing”
Ayaz Malik
Excellence Operations Enterprise Marketing, Roche
“It’s important to recognize that MLR review is a requirement for all life sciences companies. It’s critical to focus the resources we have to manage the process efficiently for all stakeholders, while ensuring we support the business in all our initiatives compliantly.”
