At iCAD, we are committed to unconditional observance of all internal and external procedures, laws and regulations that govern our business practices. As a company, we continuously work to raise awareness of compliance throughout our organization.
The Digital Imaging and Communications in Medicine (DICOM) 3.0 standard facilitates interoperability of medical imaging equipment. It is an evolving standard maintained by the ACR (American College of Radiology) and NEMA (National Electrical Manufacturers Association) in an effort to facilitate the communication of certain types of information between computers used in medical imaging.
In support of DICOM interoperation, iCAD adheres to the following:
Declarations of Conformity
IHE Integration Statements
The following IHE Integration Statements describe the specific IHE capabilities (functionality and workflow) for iCAD products used in the medical imaging market.
Health Canada Licenses
PowerLook AMP® DICOM Conformance Statement PDF 1.55 MB
SecondLook® 300 DICOM Conformance Statement PDF 303 KB
TotalLook® DICOM Conformance Statement PDF 208 KB
RoHS Declaration of Conformity
iCAD is committed to Quality, Integrity, Service and Innovation.
Deliver the highest quality products and continuously improve the effectiveness of our Quality Management System, our products and our services.
Respect for our people, our products, our customers and our partners.
Deliver the highest standard of customer service.
Advance and facilitate innovation to deliver novel healthcare technologies and services to our customers.
CAD is committed to corporate sustainability and to making a difference for our environment.
iCAD delivers innovative cancer detection and radiation therapy solutions and services that enable clinicians to find and treat cancers earlier and while enhancing patient care. iCAD offers a comprehensive range of upgradeable computer aided detection (CAD) and workflow solutions to support rapid and accurate detection of breast, prostate and colorectal cancers.
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