This version of the form is not currently in use and is provided for reference only. Download this version of Form FDA1932A for the current year.
This is a legal form that was released by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration on August 1, 2018 and used country-wide. As of today, no separate filing guidelines for the form are provided by the issuing department.
Q: What is Form FDA1932A?
A: Form FDA1932A is a report used to report adverse drug reactions, lack of effectiveness, or product defects for veterinary drugs.
Q: Who can use Form FDA1932A?
A: Form FDA1932A can be used by veterinarians, animal owners, and other concerned parties to report adverse drug reactions, lack of effectiveness, or product defects for veterinary drugs.
Q: What types of events can be reported using Form FDA1932A?
A: Form FDA1932A is used to report adverse drug reactions, lack of effectiveness, or product defects related to veterinary drugs.
Q: How should I fill out Form FDA1932A?
A: Form FDA1932A should be filled out with detailed information about the adverse drug reaction, lack of effectiveness, or product defect, including information about the animal, the drug, and the event.
Q: Is it mandatory to report adverse drug reactions, lack of effectiveness, or product defects using Form FDA1932A?
A: Reporting adverse drug reactions, lack of effectiveness, or product defects using Form FDA1932A is encouraged but not mandatory.
Q: What happens after I submit Form FDA1932A?
A: After submitting Form FDA1932A, the information will be reviewed by the FDA to determine if further action is necessary.
Q: Can I submit Form FDA1932A anonymously?
A: Yes, you can submit Form FDA1932A anonymously if you prefer not to provide your personal information.
Q: Is there a deadline for submitting Form FDA1932A?
A: There is no specific deadline for submitting Form FDA1932A, but it is recommended to report events as soon as possible.
Form Details:
Download a fillable version of Form FDA1932A by clicking the link below or browse more documents and templates provided by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration.