OUR QUALITY POLICY STATES:

“IVD Research, Inc. and SafePath® Laboratories, LLC will develop, manufacture and sell its own line of in vitro diagnostics, which meet or exceed the performance of similar in vitro diagnostics in the marketplace. In addition, will provide contract development and/or manufacturing services which fulfill customer expectations and requirements.

IVD Research, Inc. and SafePath® Laboratories, LLC commit to comply with all applicable ISO 13485:2016, statutory and regulatory requirements, and to maintain the effectiveness of the Quality Management System.

Our commitment will be measured with quality objectives which are designed to track customer satisfaction and ensure quality products are delivered. These objectives, and this quality policy, will be reviewed for continuing suitability and shared with our employees.”

STANDING BEHIND OUR STATEMENTS

We take our quality policy very seriously – in fact, we’ve built our entire business model around it. Our vision for the future of IVD Research, Inc. is to continue to grow upon our existing product offerings, as well as to enter into new markets around the globe by expanding on our already comprehensive quality systems. We strive to improve patient care while developing the next generation in diagnostics.

In addition to being registered by the California and Federal FDA, following cGMP and having products CE Marked, IVD Research, Inc. also holds an ISO 13485 certification. Our expert team, solid infrastructure, and respected distributors around the world ensure the highest level of quality, accuracy, and customer service.

Additionally, our sister company SafePath® Laboratories is a USDA Licensed Biologics Manufacturer.

IVD Research, Inc. products

DFA (Direct Immunofluorescence Assay)

IVD - Cryptosporidium/Giardia Fecal Direct Fluorescent Antigen Detection Kit