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# 2 Veterinary Medicine Guidances Published
- URL: https://www.fdaweb.com/2-veterinary-medicine-guidances-published/
- Published: 2024-02-01T12:00:00.000Z
- Updated: 2026-09-14T14:21:57.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5156269

The Center for Veterinary Medicine has published two data element guidances. The first guidance, [*Data Elements for Submission of Veterinary Adverse Event Reports to the Center for Veterinary Medicine*](https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cvm-gfi-188-data-elements-submission-veterinary-adverse-event-reports-center-veterinary-medicine?ref=fdaweb.com), is to help applicants and non-applicants to complete form FDA-1932, “Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report.” The document says applicants must report adverse drug experiences and product/manufacturing defects on that form. It says the agency has revised form FDA-1932 as part of its effort to harmonize its adverse event regulatory reporting data elements with those of other nations as well as *streamline* reporting for product and manufacturing defects.

The second guidance, [*Pharmacovigilance of Veterinary Medicine Products: Electronic Standards for Transfer of Data*](https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cvm-gfi-214-vich-gl35-pharmacovigilance-veterinary-medicinal-products-electronic-standards-transfer?ref=fdaweb.com), provides recommended standards to construct a single adverse event report electronic message to transmit to all Veterinary International Conference on Harmonization member regions and product problem reports to FDA for veterinary medicinal products.