Tag: veterinary
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FDA Extends Comment Period for Risk Assessment of Animal Drug Residues in Milk
Citing stakeholder concerns over insufficient time to develop meaningful submissions, the U.S. Food and Drug Administration (FDA) has extended by 90 days the period in which to submit comments about the agency’s risk assessment titled, “Multicriteria-Based Ranking Model for Risk Management of Animal Drug Residues in Milk and Milk Products.” FDA seeks suggestions for improving…
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Public Interest Groups Sue FDA over Animal Drug Approvals
The Center for Food Safety and two other public interest organizations have filed a lawsuit against the U.S. Food and Drug Administration (FDA) seeking to overturn its approval of 11 animal drugs containing ractopamine hydrochloride on the ground that the agency failed to undertake the analysis purportedly required under the National Environmental Policy Act (NEPA)…
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SHB Public Policy Group Spearheads Victory in Texas Supreme Court on Damages in Pet Injury Cases
SHB’s Public Policy Group recently contributed to a favorable outcome for animal medicine manufacturers in the Supreme Court of Texas, which ruled in Strickland v. Medlen that emotion-based damages, including loss of companionship and sentimental damages, are not permitted in pet injury claims in Texas. Presenting on behalf of amici during oral argument, SHB Partner Victor Schwartz…
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DOJ Charges Kentucky Cattle Company for Falsifying Records
The U.S. Department of Justice (DOJ) has reportedly indicted a London, Kentucky-based cattle company and its treasurer for falsifying records related to a federal investigation and creating false documents. The charges apparently arise out of a Food and Drug Administration (FDA) investigation to determine whether the company was violating a 2006 court-ordered injunction requiring it…
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FDA to Revise Tolerances for Residues of New Animal Drugs in Food
The Food and Drug Administration (FDA) has issued a proposed rule that would update tolerances “for residues of approved and conditionally approved new animal drugs in food by standardizing, simplifying, and clarifying the determination standards and codification style.” According to FDA, the regulations describing how to set animal drug tolerances for human food are not…
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FDA Extends Comment Deadline on Proposed Animal Drug Reporting Scheme
The Food and Drug Administration (FDA) has extended the comment period for an advanced notice of proposed rulemaking (ANPR) that announced potential changes to regulations governing new antimicrobial animal drug reporting. The ANPR proposed altering these regulations to incorporate the requirements of section 105 of the Animal Drug User Fee Amendments of 2008 (ADUFA 105).…
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FDA Announces 2012-2016 Food and Veterinary Medicine Strategic Plan
The Food and Drug Administration (FDA) recently announced the availability of its draft Foods and Veterinary Medicine Strategic Plan 2012 – 2016, which takes into account “all of the activities within the jurisdictions of the Center for Food Safety and Applied Nutrition and the Center for Veterinary Medicine and includes activities supported by the Office…
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USDA Abandons Animal ID System for New Framework
The U.S. Department of Agriculture (USDA) has announced its intention to abandon the National Animal Identification System (NAIS) and develop a “new, flexible framework for animal disease traceability,” citing public feedback and input from states, tribal nations, industry groups, and small and organic farmers. Created in 2004, NAIS aimed to register all domestic livestock in…