U.S. Senator Amy Klobuchar announced last week that she has sent a bipartisan, bicameral letter to Food and Drug Administration (FDA) Commissioner Margaret Hamburg regarding concerns over the agency’s approval process for medical devices.
A Minnesota delegation of lawmakers sent a letter to the commissioner of the Food and Drug Administration (FDA) seeking an explanation for the increase of hurdles and delays faced by companies seeking approval for medical devices.
U.S. Senator Amy Klobuchar is urging the U.S. Food and Drug Administration (FDA) and the pharmaceutical industry to address a growing shortage of prescription medications, especially drugs for treating cancer.
Following the release of a new medical report last week, U.S. Senator Amy Klobuchar continued to press the Food and Drug Administration (FDA) to reform the approval process for medical devices to maintain safety and encourage innovation.
U.S. Senator Amy Klobuchar today renewed her call for the passage of food safety legislation pending in the Senate following a recent salmonella contamination that has caused a recall of over 550 million eggs.
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