# 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Studies To Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1); Draft Guidance for Industry; Correction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:**
The Food and Drug Administration (FDA or Agency) is correcting a notice that appeared in the *Federal Register* on May 23, 2024. The 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, *[email protected].*
**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, *[email protected]* .”
Dated: June 10, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.