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    Solutions

    Functional  Service Provider (FSP)

    Helping you augment your team with hard-to-find experts. 

    Clinical study leaders in small and mid-sized biotech organizations work with Veristat to solve their capacity challenges across all functions of novel drug development. We supply hard-to-find and highly skilled scientific experts that seamlessly complement and integrate into your in-house teams, processes, and environments.

    Backed by the strength of a world-class CRO with 30 years of experience in clinical trial planning and execution for novel therapies, our scientific experts can help you manage the ebb and flow of your workforce needs with solutions tailored to your study, project budget, and business goals.

    Ready to fill your team gaps? 

    Submit Your RFP     Talk to a Resourcing/ FSP Expert

    Manage Your Resources Exactly When and Where You Need

    Demand-driven functional Resourcing

    Tailored, demand-driven functional resourcing from Veristat ensures that your focus remains on meeting milestones and accelerating time to market.

    • Connect with a Resourcing/FSP Expert Today.

      We know there are always unknown challenges when bringing a novel therapeutics to market, so we’ve  assembled an extraordinary team of scientific minded experts who have mastered the complexities of therapeutic development enabling sponsors to succeed in extending and saving lives.

     

    •  

    FSP and strategic resourcing for drug and biologic development

     

    Learn How Veristat's FSP Capabilities Can Minimize the Risks of Failure and Missed Milestones.

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    Dedicated Resources that Seamlessly Integrate into Dynamic Clinical Environments

    Our service-oriented experts will rapidly fill your skills gap and augment your team so that your most complex activities and projects advance at full speed.

    We help find you the right staff in the following disciplines:

    • Biostats/Programming & Data Management

    • Regulatory Consulting

    • Clinical Operations

    • Medical/Regulatory Writing

    • Pharmacovigilance/Safety

    Common Sponsor Challenges:

    • Sourcing hard-to-find expert in clinical operations for novel therapies 

    • Integrating a team to support patient accrual rates while maintaining data submission timelines 

    • Securing Regulatory Affairs lead to take Sponsor through to NDA submission 

    • Progressing a stalled trial 

    • Deploying medical writers on a rolling basis 

    • Reducing activation times for clinical trial sites 

    • Accelerating a database build 

    Veristat Results Delivered:

    • Capacity gaps filled with fully-vetted expert resources 

    • Business-as-usual for mission-critical work 

    • Dedicated on-site skill set  

    • Scale-up/scale down flexibility 

    • Compliant, rigorous, repeatable processes 

    • Hard-to-find experts in medical writing, statistical analysis, clinical trial reporting

    • Clear study planning

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