The Medical, Legal, and Regulatory (MLR) process is critical for life sciences organizations, especially when it comes to reviewing and approving promotional materials, scientific content, and other regulatory submissions. It ensures compliance while keeping up the pace required in getting these materials to market. During the recent
Indegene Digital Summit 2024, industry experts gathered to address critical questions such as: How can life sciences organizations streamline their MLR process without compromising compliance? Is it possible to reduce review layers while maintaining quality and regulatory adherence?
