Department of Health and Human Services February 11, 2005 – Federal Register Recent Federal Regulation Documents
Results 1 - 18 of 18
International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH); Final Guidance for Industry on Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: General Approach to Establish a Microbiological ADI (VICH GL-36); Availability
The Food and Drug Administration (FDA) is announcing the availability of a guidance document for industry (159) entitled ``Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: General Approach to Establish a Microbiological ADI'' (VICH GL36). This guidance has been developed for veterinary use by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH). This VICH guidance document provides guidance for assessing the human food safety of residues from veterinary antimicrobial drugs with regard to effects on the human intestinal flora.
Annual Comprehensive List of Guidance Documents at the Food and Drug Administration; Correction
The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of January 5, 2005 (70 FR 824). The document provided the agency's annual comprehensive list of guidance documents. The list provided information on current guidance documents and those that have been withdrawn. The document was published with some inadvertent errors. This document corrects those errors.
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