Webinar - MLR of the future: Accomplish review, approval and delivery in <24 hours
Rapid innovation and higher rate of regulatory approvals, in the life sciences industry, have led to faster product launches and increase in product-related content volumes. Likewise, information consumption patterns of HCPs and patients have moved towards on-demand, personalized, and real-time digital content. Organizations are relying on digital channels to reach target audience– more than they ever did.
The result- content proliferation, thereby putting pressure on MLR review teams to deliver more content and at a much faster rate.
We believe that, in near future promotional content will need to be reviewed and published to market in less than 24 hours post authoring. Organizations that can truly deliver compliant content on-demand will undoubtedly have an advantage over competition.
What you will learn
Roadmap to prepare for the future of material reviews
Role of AI in driving productivity and cost efficiencies for material review
Best practices in leading organizations to achieve faster, high quality, and compliant content
Eli Lilly and Company