Accelerating Study Start-up with an innovative outsourcing solution

Event overview

The pharma industry is facing an ever-increasing pressure to reduce clinical trial cycle times and complete studies with the utmost speed and efficiency. In order to support the reduction of white space within start-up it is essential that consideration is given to planning, resourcing, technology and processes.

In this latest webinar from IQVIA FSP our team of clinical FSP specialists will walk you through how to traverse the volatility in starting up a trial and forecasting what is required to ensure a speedy delivery and set-up. We’ll highlight how the need for in-depth resource forecasting including task navigation and building the right team structure with the right skills and knowledge are imperative in study start-up.

We’ll also outline where applying co-design processes, technology, and being able to measure success add value to your outsourcing partnerships.

Three key take-aways

• Providing realistic planning, consistency, and measurements by utilizing the benefits FSP of a partnership
• When and where to add “co-design” and technology to enhance study start-up
• Learn the importance of how to structure study start-up in an outsourced partnership that leads to great efficiency, speed, and trial development.