Sponsored Webcast: Leveraging Today’s Technology to Accelerate Submissions: Real Life Examples and Lessons Learned (On Demand)
As the drug development industry strives to accelerate submission timelines and improve patient access to healthcare solutions, regulatory professionals are increasingly pressured to leverage technology to go faster. During this webinar, Heather Graham, Vice President of Regulatory Science and Medical Affairs at Certara, will facilitate a panel comprising industry experts to discuss the current technology landscape, how these technologies can be leveraged to accelerate high-quality, fit-for-purpose submissions, and how effective change management is critical in implementing technology across an organization.
Registration Fees & Deadlines
Free
Learning Objectives
- Attendees will understand the different types of technology being used to accelerate regulatory submission preparation.
- Attendees will learn about real-life examples of where and how these technologies were leveraged in submission preparation
- Attendees will learn about organizational change management approaches as new technology is embedded in existing processes.
Who Should Attend?
Regulatory professionals who are involved in regulatory content generation and management in support of regulatory submissions.
Learning Level
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
