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AMDL, Inc. Enters Into Distribution Agreements With GenWay Biotech, Inc. to Advance Commercialization of the DR-70 (FDP) Cancer Test in the US and Canada
Date:5/13/2009

ncer test in the US and Canada. AMDL has developed a highly-effective test to provide potentially life-saving information regarding cancers and we are excited to bring it to the US and Canada."

DR-70 (FDP) is an in vitro diagnostic test that enables physicians and their patients to effectively monitor and/or detect certain types of cancers by measuring the accumulation of specific breakdown products in the blood called Fibrin and Fibrinogen Degradation Products (FDP). FDP levels rise dramatically with the progression of cancer. DR-70 can be used as a simple, non-invasive blood test to monitor and/or diagnose the progression or status of certain cancers. The Company received US FDA approval for DR-70 in the second quarter of FY2008 and began executing a commercialization strategy for the product late in the fourth quarter of the same year.

DR-70 has been approved by the US FDA for the monitoring of colorectal cancer and by Health Canada as a lung cancer screen and cancer monitoring tool. Following the introduction of the DR-70 (FDP) cancer test in the US and Canada, AMDL intends to expand product commercialization to select international markets based on other regulatory approvals and plans to file for marketing approvals in other areas of the globe.

For additional information on AMDL and its portfolio of products visit the Company's corporate website at www.amdl.com. For Investor Relations information contact Kristine Szarkowitz at kszarkowitz@amdl.com or 1.206.310.5323.

About AMDL:

Headquartered in Tustin, CA with operations in China, AMDL, Inc., along with its subsidiary Jade Pharmaceutical Inc. (JPI), is a pharmaceutical company devoted to the research, deve
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