Data Capture Software for
MedTech Innovators

You innovate,

CRISP documents

Innovating medical products is exciting and stimulating. Documenting your work is not.

This motivated us to develop CRISP, a dedicated software for documenting your product development activities.

“If it is not documented,

it does not exist”

Gaps in the documentation are costly...

Unverifiable data, loss of critical knowledge, poor decision making, and the need to re-track, re-search, re-do, and re-test.

CRISP Makes Data Capture

Quick and Easy

Dedicated software modules capture all development activities from Day 1.

Configure, select, upload, hyperlink. CRISP takes care of the rest.

CRISP Organizes and Links

Your Documents

Concepts, prototypes, testing, voice of customer, root cause analysis, and more...

Everything is in one place.

CRISP Takes Your Concept on a

Virtual Test Drive

Take a virtual test drive through the entire use life of your product to identify user tasks, design requirements, critical operating conditions, safety hazards, and safety measures.  CRISP converts the captured information into trace matrices.

CRISP Builds a

Comprehensive Design History

CRISP issues professional reports and catalogues them chronologically. Your entire design history is just a mouse click away.

CRISP Guides Your Design Process

From Day 1

Incubate

CRISP guides you through an in-depth performance and risk assessment.

Universal

CRISP can be configured to any type of medical product.

Comprehensive

CRISP helps to identify design requirements and hazards throughout the entire product use cycle.

Accelerate

CRISP helps you in selecting the best design solution.

Agile

CRISP supports the parallel evaluation of alternative design options.

Design-Centric

The CRISP health report identifies information gaps and design risks

Realize

CRISP supports the product development process all the way to first-in-human.

First-in-human

CRISP integrates the clinical protocol, product release, and investigator training into the performance and safety assessment.

Seemless

CRISP generates design requirement and hazard trace matrices for a seemless transition into QMS.

Welcome!

Request a DEMO and experience the unique features of CRISP

CRISP, the software for Continuous Risk and Performance assessment of medical devices. Patent pending technology developed by DualTrack, LLC.