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On average, most pharmacy boards have five inspectors responsible for visiting all the pharmacies in the state. Budgets vary greatly from state to state, with Nevada providing $3,000 in funding for each pharmacy in the state and Indiana providing with less than $200 per pharmacy. Only 19 states train inspectors to recognize problems with sterile compounding, which is considered the riskiest type of compounding because it requires highly sanitary conditions and complicated production techniques. "This report clearly indicates what we've known for quite some time
-- that there is no clear, functioning, or uniform process for all 50 states to manage and oversee compounding pharmacies," said Rep. John Dingell, D-Mich., in a statement. Dingell's office helped conduct the survey. The findings will likely come into play on Tuesday, when a House investigative committee holds its second hearing on the meningitis outbreak. Republicans on that committee have argued that the FDA could have shut down the NECC using its existing powers. Lobbyists for the compounding industry generally share that view, and have fought proposals to give the federal government more authority over compounding for decades. Last week House Democrats released dozens of documents from the International Academy of Compounding Pharmacists, the industry's leading trade group. The documents include internal memos to members suggesting how they deal with FDA inspectors, in particular: "when a pharmacist should NOT provide certain information to the FDA," and "when pharmacists should draw the line and discontinue the visit and call their attorney." Democrats on the House Energy & Commerce Committee suggested the CEO of the trade group should testify at Tuesday's hearing. However, Democratic staffers said late last week they had not received a response on that request from Republicans, who control the chamber. FDA Commissioner Margaret Hamburg is schedule to testify.
[Associated
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