89 FR 117 pgs. 51352-51353 - International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products; Studies To Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1); Draft Guidance for Industry; Correction

Type: NOTICEVolume: 89Number: 117Pages: 51352 - 51353
Docket number: [Docket No. FDA-2000-D-0784]
FR document: [FR Doc. 2024-13224 Filed 6-14-24; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version:  PDF Version
Pages: 51352, 51353

[top] page 51352

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2000-D-0784]

International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products; Studies To Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1); Draft Guidance for Industry; Correction

AGENCY:

Food and Drug Administration, HHS.

ACTION:

Notice; correction.

SUMMARY:


[top] The Food and Drug Administration (FDA or Agency) is correcting a notice that appeared in the Federal Register on May 23, 2024. The page 51353 document announced the availability of a draft revised guidance for industry (GFI) #115 (VICH GL22) entitled "Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1)." The document erroneously included incorrect contact information. This document corrects that error.

FOR FURTHER INFORMATION CONTACT:

Li You, Center for Veterinary Medicine (HFV-153), Food and Drug Administration, 7500 Standish Place, Rockville, MD 20855, 240-402-0828, Li.You@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

Correction

In the Federal Register of May 23, 2024 (89 FR 45663), in FR Doc. 2024-11313, on page 45664, in the first column, correct the FOR FURTHER INFORMATION CONTACT section to read "Li You, Center for Veterinary Medicine (HFV-153), Food and Drug Administration, 7500 Standish Place, Rockville, MD 20855, 240-402-0828, Li.You@fda.hhs.gov ."

Dated: June 10, 2024.

Lauren K. Roth,

Associate Commissioner for Policy.

[FR Doc. 2024-13224 Filed 6-14-24; 8:45 am]

BILLING CODE 4164-01-P