Trial activation is widely recognized as one of the most challenging aspects of clinical trial management. It involves navigating complex regulatory requirements, securing timely approvals, and coordinating with multiple stakeholders. Delays in study activation can lead to increased costs, resource inefficiencies, and extended time-to-market for novel treatments.

Vitalief offers comprehensive Rapid Trial Activation Services designed to optimize site operations and accelerate study start-up timelines. Our approach begins with a thorough assessment of your current processes, followed by the development of a customized roadmap to address your unique challenges.

Post-assessment, we provide actionable recommendations that you can implement independently, or we can partner with you throughout the implementation process to ensure seamless execution.

Our solutions include:

• TRIAL ACTIVATION ASSESSMENT AND ROADMAP
  We evaluate your site’s capabilities, create a tailored roadmap, and implement innovative strategies to enhance trial activation. Based on our assessment, we may propose a shift to a more efficient outsourcing approach or streamlined workflows.
• TRIAL ACTIVATION ROADMAP IMPLEMENTATION
  We help you implement the recommended strategies and activities to fuel rapid trial activation. 
• SITE AND TRIAL FUNCTIONAL SERVICE PROVIDER (FSP) SOLUTIONS
  Whether you need to outsource individual roles, specific trials, or the entire function, our FSP services provide flexible, scalable support to meet your operational needs.
  As a result of a Trial Activation Assessment and Roadmap, we may deploy a Rapid Trial Activation team to address trial backlogs while we help your team implement updated tools and processes. This approach enables Site teams to kickstart trial activation and see short-term progress toward goals.

With Vitalief, Sponsors, CROs, and Sites gain the expertise, resources, and support needed to improve trial start-up efficiency, and deliver exceptional results.