Doctors looking at screen
Explanation of trial setting for Imaging CROs and Pharma companies

Data Management

Project Management

Radiological Read

Explanation of trial setting for Imaging CROs and Pharma companies

Data Management

Project Management

Radiological Read

mint Lesion TM for Sponsor Initiated Trials

 

mint Lesion™ is designed to facilitate research in clinical trials with imaging endpoints. This includes the transfer and storage of clinical trial DICOM data, a workflow optimized for consistent interpretation and reviewing of image findings, the reviewing of image meta-data, and the simplified provision of results to physicians and other clinical systems, e.g. PACS and Clinical Trial Management Systems. mint Lesion™ thus implements the functionality of a Clinical Trial Image Management System (CTIMS) as defined by the NCI.

Explanation of workflow diagramm

Project Management

 

mint Lesion™ allows you to model the needs of your imaging charter by software configuration. Have dedicated medical experts, tasks, workflows, and permissions set up and let mint Lesion drive your imaging research – from image quality assurance and eligibility read up to patient cohort level data export and reader metrics.

Objective Radiological Read

 

The context-driven read procedures of mint Lesion™ will guide the radiological expert to perform a dedicated assessment in an optimized read context. Significant observations in morphologic and functional image data are documented and classified in adherence to the protocol and tracked throughout treatment. By this means, mint Lesion™ provides the basis for a true objective assessment and minimizes reader variability. Let mint Lesion help your readers to speed up their work and focus on their job-to-be-done.

Screenshot of general radiological read
Explanation of Case Tasks Management

Monitoring & Data Management

 

Monitoring project progress directly within mint Lesion™ will increase the efficiency of your research work. As one example, corrective actions are managed, performed, and documented in immediate correlation with the image annotations to assure traceability and integrity of your research data. Comprehensive and high quality data is crucial in clinical research. mint Lesion™ generates this data for a single observation on image data up to comprehensive data exports for the entire study cohort. An automated response assessment automatically assigns the time-point response from lesion measurements and classifications to avoid manual calculations.

Make mint Lesion™ a perfect fit for your particular project’s needs by an optimum customization using our configurable criteria and workflow engine

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HIGHLY CUSTOMIZABLE
WORKFLOWS

Benefit from an integrated image reviewing for blinded readers that comprises comprehensive edit checks to assure full adherence to our study protocol

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VALIDATED
INDEPENDENT READS

Achieve high quality research results with mint Lesion™, the single dedicated Clinical Trial Imaging System in line with CFR Part 11, GxP, and HIPAA as approved medical device
(FDA 510k, CE)

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FULL REGULATORY
COMPLIANCE

Safe time and efforts in clinical trial operations and data management with the help of mint Lesion™’s comprehensive and flexible interfaces to CTMS, EDS and other systems

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SEAMLESS
INTEGRATION

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IN NUMBERS
102

Phase 1 Trials

78

Phase 2 Trials

19

Phase 3 Trials

17913

Overall approved reads

HOSTING
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Cloud-hosted

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On-premise