Accelerating Study Start-Up to Improve Research Site Success

Timelines for study start-up affect everything from budgets and drug pricing to a site’s ability to secure trials. This webinar will provide actionable strategies to streamline start-up processes, accelerate regulatory approvals, and optimize patient recruitment. By adopting these best practices, sites can reduce delays, improve trial timelines, and strengthen their competitive edge.

Learning Objectives:

1. Discuss the importance of start-up speed in clinical research and its direct impact on trial timelines and success.
2. Integrate insights into actionable strategies and best practices to accelerate start-up processes and streamline regulatory approvals.
3. Review tactics to leverage accelerated start-up phases to enhance efficiency, minimize delays, and optimize patient recruitment.

Christine Senn

Senior Vice President, Site-Sponsor Innovation, Advarra