JMP® Clinical

Clinical data analysis software for ensuring trial safety and efficacy

Role-based workflows, reusable templates and automated reporting tools make it easy for all key participants in the trial review process to explore trends and outliers and share results. Capabilities including RECIST-based oncology visualizations, risk-based monitoring, data monitoring and statistical analysis limit costly on-site reviews and reveal hidden data, safety and efficacy issues.

Request an evaluation of JMP Clinical

Have a minute? See JMP Clinical in action.

Clinical data scientists and medical monitors

Summary dashboards in JMP Clinical enable medical reviewers to evaluate safety and efficacy issues with the click of a button. Create interactive reports of adverse events, concomitant medications, labs and vital signs, and drill down to customized patient profiles and patient narratives.

Medical writers

Producing adverse event narratives for clinical study reports (CSRs) can be a painstaking, time-consuming process with significant consequences for inaccuracies or delays. With JMP Clinical, medical writers can automate patient profiles and patient narratives and reduce the time and complexity of creating output for review and submission to regulatory agencies.

Clinical operations

The goal of clinical operations is to mitigate data quality risks that could hinder a regulatory submission or drug approval. Risk-based monitoring tools in JMP Clinical help you identify data anomalies at the vendor, monitor, site and country level, and determine the factors responsible for lapses in safety or data quality.

Data managers

Scrupulously maintaining the validity of all data throughout the trial process is crucial. JMP Clinical helps data managers visually monitor the status of all data and quickly identify new, modified, deleted or duplicate data. This lets you expedite database locking and ensures that downstream analysis will always be based on valid data.

The Core Capabilities of JMP Clinical®

  • Patient Narratives

    Automatically compose a configurable patient narrative for each subject who experienced an adverse event (AE), including reporting for deaths, serious AEs, AEs of special interest and AEs resulting in study discontinuation.

  • Patient Profiles

    Instantly generate customizable patient profiles and easily communicate findings among review groups.

  • Risk-Based Monitoring

    Reduce costly on-site source data verification while preserving data integrity and the safety of study participants.

  • Data Integrity

    Discover data anomalies at the site and patient level, whether due to fraud, data quality or protocol errors.

  • Data Management

    Visually identify modifications to data and isolate data entry and EDC errors for downstream users of the data.

  • Data Visualization and Analysis

    Reveal trends and outliers and accelerate discovery via interactive visualization and sophisticated pattern detection.

  • Tumor Response Analysis

    Quickly identify efficacy signals in solid tumor clinical trials using visualizations tailored to RECIST criteria, including survival plots, swimmer plots, waterfall plots and spider plots.

  • Data Monitoring

    Assess trial data for safety issues with the click of a button and create interactive reports of adverse events.

  • Biometrics and Biostatistics

    Dig deep into clinical trial events, findings and interventions using sophisticated statistical algorithms.

  • Interventions

    Track patient exposure to treatment, identify drug interactions, and analyze distributions, event rates and risk.

  • Events

    Determine the onset of an adverse event and its outcomes, and discern event patterns across treatment groups.

  • Findings

    Quickly evaluate efficacy and safety, and identify potentially harmful symptoms, including liver toxicity.

Back to Top