Epitope Diagnostics, Inc.

7110 Carroll Road, 92121 San Diego, CA
United States of America
Telephone +1 858 693-7877
Fax +1 858 693-7678
cs@epitopediagnostics.com
http://www.epitopediagnostics.com

Product Categories

03 Diagnostics
03.02 Immunochemistry (Immunology)
03.02.14 Specific proteins
MEDICA 2017
Specific proteins

Anti-Auristatin Monoclonal Antibodies
1 Product

03 Diagnostics
03.02 Immunochemistry (Immunology)
03.02.15 Rapid tests - Immunochemistry
MEDICA 2017
Rapid tests - Immunochemistry

Human Anti-Gliadin IgA ELISA Kit
1 Product

03 Diagnostics
03.02 Immunochemistry (Immunology)
03.02.17 Tumor markers
MEDICA 2017
Tumor markers

Human Pepsinogen II ELISA Kit
1 Product

03 Diagnostics
03.05 Infectious Immunology
03.05.06 Parasitology (Infectious immunology)
MEDICA 2017
Parasitology (Infectious immunology)

03 Diagnostics
03.05 Infectious Immunology
03.05.08 Rapid tests - Infectious immunology
MEDICA 2017
Rapid tests - Infectious immunology

Human Anti-Gliadin IgA ELISA Kit
1 Product

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Company

Company details
Epitope Diagnostics Inc. (EDI) strives to develop, manufacture, and market the highest quality and most innovated in-vitro diagnostics (IVD) products to the global research, pharmaceutical, and healthcare community. We seek to become a major contributor in resolving the unmet medical needs of the world.

History
Located in America's finest city and one of the biotech hubs of the U.S., Epitope Diagnostics, Inc. was established in 2003. Since then, EDI has developed and launched many innovative ELISA and rapid test kits that meet the needs of healthcare communities worldwide. For instance, EDI launched the world's first commercial test for the determination of alpha-1-HS-glycoprotein, the human fetuin-A ELISA kit. Many clinical studies were performed using this test which led to the publication of more than 20 scientific papers.

In 2004, EDI was accredited by the State of California Department of Health Services, Food and Drug Branch, as a certified and licensed medical device manufacturer. A year later, EDI developed and innovative, odorless, and self-contained rapid test platform specifically for stool sample-based rapid tests. This innovative device has been patented (US 7,780,915), FDA 510(k) cleared, and CLIA-waived since 2005. This platform has gone on to be the basis of all our rapid test kit, including the European CE certified OTC kit, EpiTuub iFOB test.

ISO Certification
EDI is an ISO 13485:2003 certified company.

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