IRVINE, California and AMSTERDAM, October 3, 2011 /PRNewswire/ --
Agendia, an innovative molecular cancer diagnostics company, today announced that the company successfully completed a recent, routine inspection of its Irvine, California-based laboratories by the US Food and Drug Administration (FDA). Agendia received FDA 510(k) clearance for its MammaPrint® breast cancer recurrence test in early 2007. It remains the first and only test of its kind to receive FDA clearance, which, in addition to validiation of the product's safety and efficacy, periodically subjects the company's laboratories to the scrutiny of FDA inspectors to ensure continuous compliance with regulations.
"Agendia was founded on the principle of providing safe and effective products to improve patients' quality of life, and we have gone to great lengths to ensure that MammaPrint meets this high standard," said Dr. Bernhard Sixt, CEO and co-founder of Agendia. "Ensuring the safety of MammaPrint doesn't just stop at the approval process. We must ensure that MammaPrint continues to comply with regulations throughout the life of the test. This is why we sought FDA clearance and why we believe the industry, as a whole, should be regulated in the same manner. I am immensely proud that FDA has once again validated Agendia's MammaPrint test and take even greater pride to offer the only breast cancer recurrence test that has been subjected to such painstaking FDA oversight."
FDA inspectors thoroughly examined Agendia's facilities, evaluating the company's compliance with FDA's Good Manufacturing Practice Regulations (GMP), which require manufacturers of drugs, medical devices and FDA cleared laboratory tests to ensure product safety and effectiveness. GMP regulations compel companies, such as Agendia, to employ strong manufacturing practices that minimize or eliminate the risk of contamination, laboratory mixups and errors. FDA inspectors assessed Agendia's laboratory op
|SOURCE Agendia B.V.|
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