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Precision 360° Intelligence for insights in every direction of development

Gain a 360° view of your clinical trial data ecosystem, from sample collection and translational science to clinical data management and statistical programming.

Leverage the world’s first ecosystem of Precision large language models (LLMs) and purpose-built AI-enabled intelligence tools for transforming and visualizing clinical data to provide a 360° look at your trial data ecosystem.

Built to drive value for people, across the R&D lifecycle, our technology solutions centralize oversight at the patient, site, study and program level and provide actionable data visualizations, ultimately delivering hope to patients in need.

 

 

Biomarker intelligence

QuartzBio® Software-as-a-Service (SaaS) products connecting biospecimen, assay, and clinical data sources

From sample collection to biomarker data management, our end-to-end suite of products enables sponsors to gain insights from information. We connect biospecimen, assay, and clinical data sources in a secure, scalable, cloud-based infrastructure. Our products enable automated data management workflows, key insight development, improved collaboration, and more informed decisions.

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    virtual Sample Inventory Management (vSIM)

    Digitally monitor the status of biospecimens and their informed consent across multiple sites, labs, and repositories over the entire sample lifecycle.

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    enterprise Biomarker Data Management (eBDM)

    Acquire, QC, and transform all your biomarker data, including exploratory data, preclinical data, and public repositories—connected to sample and clinical data—across your enterprise.

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    AI Virtual Assistant

    Conversationally interrogate your sample and biomarker data ecosystem with this first-in-class technology. Our Virtual Assistant transforms and accelerates how teams access, interact with, and extract value from their data, powered by the first ensemble of Precision Medicine LLMs.

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Clinical intelligence

Precision's clinical data intelligence technology solutions accelerate data-centric drug development to enables clients to make cost-effective treatments available to patients faster. Our proprietary programming and visualization tools support clients' workflows in clinical data management, statistical programming, biometrics, and biostatistics.

  • Legacy data conversion

    MetaVate

    Automate clinical data transformation from any source to any target, including SDTM, ADaM and third-party data, with machine learning-driven technology. 

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    Clarity

    Enable proactive analysis and centralized oversight at the patient, site, study and program level with powerful tools for clinical data analysis, intelligence and visualization.

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Clinical trial services empowering trial management and operations

Better visibility, better collaboration, better execution. Targeted solutions we’ve developed based on decades of experience and being at the forefront of modern drug development – focused on the opportunities to deliver the most value for your program

  • Study design and tailored statistical analysis plan
  • Clinical Data Management delivered from more than 70 team members with an average of 12 years of data management experience
  • Clinical biometrics with a 100% EU regulatory agency data acceptance rate
  • Create submission-ready data sets (including CDISC) using a secure 21 CFR Part 11 and GDPR compliant infrastructure

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    Clinical Data Management

    One dedicated team – armed with indication-specific expertise – supports your project from start-up to database lock, delivering data you can trust using the optimal EDC for your study.
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    Biostatistics

    Precision’s team of clinical biostatisticians provides trial design consultation, statistical methodology recommendations, programming expertise, and data interpretation, delivering trial results efficiently and on time.
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    Statistical Programming

    Our team of highly skilled statistical programmers consistently delivers speed, quality, and compliance, resulting in timely and successful regulatory submissions.

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