The Food and Drug Administration (FDA or Agency) is announcing that a collection of information entitled “Reporting and Recordkeeping Requirements for Human Food and Cosmetics Manufactured From, Processed With, or Otherwise Containing, Material From Cattle” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (PRA).
ACLA President to Testify on Regulation of Diagnostic Tests
Washington, D.C. – American Clinical Laboratory Association (ACLA) President Susan Van Meter will testify before the House Energy and Commerce Committee’s Subcommittee on Health for a hearing … Read More
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ACLA Statement on LDT Proposed Rule Comments by FDA and CMS
Washington, D.C. – In response to a joint release from the U.S. Food & Drug Administration (FDA) and Centers for Medicare & Medicaid Services (CMS) … Read More
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ACLA Welcomes Mary Lee Watts and Elyse Oveson to Key Positions
Washington, D.C. – The American Clinical Laboratory Association (ACLA) has welcomed Mary Lee Watts as Vice President of Government Affairs and Policy and Elyse Oveson … Read More
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FDA Proposed Rule to Regulate LDTs as Medical Devices Would Slow Development of Critical Lab Tests and Should be Withdrawn, ACLA Urges
FDA Regulation of LDTs is Misguided; Requires Congressional Authorization Washington, D.C. – The American Clinical Laboratory Association (ACLA) today submitted comments urging the U.S. Food … Read More
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