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Global Execution

Not Just FSP, FSPrecision

Agile, scalable delivery expertise, built around your needs
Traditional Functional Service Provider (FSP) models are rigid and can slow your progress. Precision FSP is built for flexibility. Whether that means adding specialized staff quickly or building strategically aligned teams for complex projects, our approach adapts to your needs, integrates with your systems, and scales as your program evolves.

Functional Service Provider Solutions

Precision elevates FSP partnerships with strategic alignment and operational excellence at every phase of clinical development. As programs progress, expertise needs and team dynamics evolve, impacting cost, timelines, and efficiency. With Precision FSP, we build delivery teams that adapt seamlessly, creating value at every stage and accelerating the path to positive patient outcomes.

Aligned Expertise

Ensure the right expertise is in place exactly when your program needs it...

We bring together specialized talent and proven processes to integrate seamlessly with your teams. From day one, our experts align with your program goals, compliance requirements, and operational workflows—ensuring precision and consistency at every step.

Collaborative Innovation

Build a partnership that supports your goals at every stage...

Collaboration drives innovation. We combine proprietary technologies with human insight to accelerate data transformation, enhance risk monitoring, and deliver smarter solutions, helping you stay ahead in a dynamic clinical landscape.

Unparalleled Agility

Respond quickly when priorities shift, without losing speed or focus...

Your needs evolve, and so do we. Our flexible engagement models allow for rapid scaling up or down without disruption. This agility ensures you maintain efficiency, control costs, and keep delivery timelines on track.

Flexible Solutions

Keep your processes intact while scaling with confidence...

No two programs are alike. That’s why our solutions are tailored to your unique requirements, from governance frameworks to operational models. We adapt to your structure, priorities, and commercial drivers to deliver measurable outcomes.

Insights to Power Your FSP Strategy

Boost project outcomes without giving up control

Expert functional teams enhance delivery while you retain full project oversight.

We manage the resourcing and execution to meet your quality and timeline standards, with the operational excellence that drives better results.

Whether support single or multiple-function projects, we align with your SOPs and systems or ours. Backed by robust three-tier governance, we deliver with reliability and precision.

Comprehensive Support, Client-Driven Management 

Expand your capabilities with Precision FSP

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    Clinical Monitoring

    Enhance your clinical trials with Precision's expert CRAs. Through proactive site management and effective communication, they foster seamless site coordination and high-quality data collection. 
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    Clinical Data Management

    Accelerate your clinical programs with our diverse pool of data management experts, well-versed in supporting the data cleaning and efficient clinical trial database design and data acquisition utilizing a variety of EDC systems.
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    Drug Safety & Pharmacovigilance

    Deliver drug safety and compliance with Precision. Meet the highest safety standards while we help you navigate the complexities of global regulatory requirements. 
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  • Patient Data Review
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    Biostatistics

    Strengthen your trials with our seasoned biostatistics team, specializing in innovative trial designs, niche therapeutic areas and extensive expertise in supporting regulatory submissions.
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    Statistical Programming

    Our global statistical programming teams bring an average 10 years of experience, having supported both drugs and device submissions to global regulatory authorities.
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    Medical Writing

    Increase the efficiency and quality of your clinical documentation with Precision's medical writing team, skilled in crafting clear, compliant, and compelling submissions. Our experts specialize in regulatory documents, clinical study reports, and patient narratives, ensuring your research communicates effectively with regulatory authorities and stakeholders.
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Robust FSP governance with Precision

Every FSP partnership is supported by a dedicated customer success ecosystem. Anchored in a strong governance framework and guided by executive oversight, we deliver transparency, reliability, and continuity, ensuring our clients experience consistent excellence across every engagement.
  • Getting Started with Precision FSP
  • Governance for Functional and Commercial Excellence
  • Scaling Operations with Precision

  • Seamless Integration from Day One

    At the outset of every collaboration, our teams align with your program structures, delivery environment, and compliance requirements to ensure seamless integration. We embed ourselves into your workflows, adapting to your goals, training protocols, and operational rhythms from day one.

    This alignment is reinforced through a multi-tiered governance structure that brings together stakeholders across levels to review key business outcome indicators and ensure strategic continuity.

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  • A Multi-Tiered Framework for Measurable Outcomes

    Governance at Precision FSP goes beyond oversight. It’s a dynamic framework designed to monitor performance metrics and KPIs with precision,  driving both delivery excellence and commercial impact. Our approach ensures that every engagement is accountable, transparent, and focused on achieving your strategic outcomes.
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  • Agility to Match Your Evolving Needs

    As your needs evolve, so does our support. Precision FSP partnerships are built to scale up or down based on your business drivers.

    Our teams are agile, responsive, and structured to align with your operational pace, efficiency goals, and commercial priorities. Whether expanding scope or streamlining resources, we ensure continuity without compromise.

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Proprietary Technologies with Human Expertise by Your Side

Precision combines advanced technology with expert oversight to accelerate delivery and enhance quality across your programs.

Metavate | Automated Data Transformation, Expert-Driven Quality 

Metavate empowers programming teams to transform data faster and submit with confidence through automated CDISC conversion backed by expert guidance:

  • One-click transformation to CDISC-compliant datasets (SDTM, ADaM) with comprehensive metadata standards 
  • Multi-study scalability with diverse data structures for transparency and reproducibility across studies 
  • Full regulatory alignment for USFDA, EMEA, and PMDA with macro-free SAS code and complete traceability
  • Expert CDISC support accelerating specification creation, dataset generation, and time to market 

Clinscope | Reveal Potential Risks Before They Impact Your Trial

Clinscope enables cross-functional teams to identify risks early and act fast with real-time clinical data intelligence across patient, site, and study levels:

  • Early anomaly detection through patient-level monitoring with visual profiles and safety triggers
  • Timely intervention with site performance tracking and key risk indicators (KRIs) for data quality oversight 
  • Progress monitoring via study-level analytics tracking milestones, budgets, and quality metrics
  • Comprehensive RBQM aligned with ICH-GCP E6 R3 guidelines for risk identification and mitigation

Read our latest Precision insights

Stay updated with the latest insights in clinical development and next-generation engagement models through our blog. 

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Read: Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies

Clinical Trials

Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies

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    Kurt Preugschat
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Read: Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM) Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

Clinical Trials

Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1754641517766, hs_published_at=1763745278294, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Kurt Preugschat
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Read: Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM) Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

Clinical Trials

Phase I Clinical Trial Designs: Bayesian Logistic Regression Model (BLRM)

|
    has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1754641517766, hs_published_at=1763745278294, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=287,height=287,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.png',altText='kurt-preugschat',fileId=194097561372}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Kurt Preugschat
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Specialized capabilities in every stage of clinical development

Leverage an integrated infrastructure that reduces the inefficiencies inherent in complex development. Integrate lab and trial execution to accelerate speed to market. Precision can customize and converge our capabilities to meet your program's unique needs—driving efficiency, agility, and success from start to finish.

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    Global CRO
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    Award-winning CRO with deep oncology and rare disease expertise

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    Global Laboratory
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    Exceptional translational and biomarker sciences with global central lab services

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