Post-Market Surveillance
Purpose-built to support your product surveillance teams, MMI offers unparalleled imaging insights for your post-market imaging on a per case basis. Our fully customizable approach allows surveillance teams to get their questions answered by independent, expert physicians and obtain unbiased imaging observations into post-market product performance.
Maven MDTM – An Imaging-Based, Post-Market Surveillance Platform
MMI understands that clinical research doesn’t end with the device or product hitting the market! That’s why we started Maven MD™, a service platform designed exclusively to support product surveillance teams in identifying and categorizing imaging-based outcomes in the context of product surveillance.
In contrast to a typically rigid clinical trial workflow, our post-market surveillance program is fully customizable to fit client requirements and preferences, offering a robust solution for review of imaging by qualified healthcare providers to assess product performance, monitor defects, and track trends to improve product design. Images are assessed on a per case basis, allowing flexibility in the timing and quantity of submissions and reports. Clients can provide product information and ask questions through the platform directly to MMI’s expert reviewers, who are board-certified, practicing radiologists that understand both the clinical and imaging aspects. Our reviewers take the time to evaluate all available information, after which they detail their imaging observations and address client questions in a final written report. MMI’s Client Services team works closely with the reviewers to ensure that each generated report adds value for our clients.
Maven MDTM – An Imaging-Based, Post-Market Surveillance Platform
MMI understands that clinical research doesn’t end with the device or product hitting the market! That’s why we started Maven MD™, a service platform designed exclusively to support product surveillance teams in identifying and categorizing imaging-based outcomes in the context of product surveillance.
In contrast to a typically rigid clinical trial workflow, our post-market surveillance program is fully customizable to fit client requirements and preferences, offering a robust solution for review of imaging by qualified healthcare providers to assess product performance, monitor defects, and track trends to improve product design. Images are assessed on a per case basis, allowing flexibility in the timing and quantity of submissions and reports.
Clients can provide product information and ask questions through the platform directly to MMI’s expert reviewers, who are board-certified, practicing radiologists that understand both the clinical and imaging aspects. Our reviewers take the time to evaluate all available information, after which they detail their imaging observations and address client questions in a final written report. MMI’s Client Services team works closely with the reviewers to ensure that each generated report adds value for our clients.
Clients can provide product information and ask questions through the platform directly to MMI’s expert reviewers, who are board-certified, practicing radiologists that understand both the clinical and imaging aspects. Our reviewers take the time to evaluate all available information, after which they detail their imaging observations and address client questions in a final written report. MMI’s Client Services team works closely with the reviewers to ensure that each generated report adds value for our clients.
WHAT WE OFFER
Fully Customizable Workflow to Support Individual Case Reviews
Easy-to-use, encrypted, web-based platform tailored specifically for product surveillance teams to upload imaging and other relevant case or product information
Expert radiologists who provide written feedback on any case images submitted
Customizable report output including prose and annotations, tailored to our client’s needs
Managed, fully customizable workflow and notification system for all users
QA/QC process to optimize accuracy and efficiency of reporting
Clinical-grade Picture Archiving and Communication System (PACS) viewer with in-platform image calibration, measurement, and annotation capabilities
Support for multiple modalities and file formats, including non-imaging information (e.g. case report forms, product information)
Experienced MMI managers for technical and logistical support
How can we help?
Want to monitor, categorize, and mine imaging data from your product users?
Need an imaging expert to determine whether product removals were device-related?
Looking for a radiologist to make sense of a complicated case history?
Don’t have uniform information across all of your cases to warrant a registry or formal study?
Let MMI provide insights into your clinical study imaging.
Have questions? We’ll connect you immediately to one of our scientific managers and imaging experts. Your time is precious, and we want to make the most out of it.
