Health

Animal Drug User Fee Act: Public Meeting and Request for Comments

🇺🇸United States··Notice·Medium Impact·View source ↗

AI-generated summary for informational purposes only. Not legal advice. See the original source for the authoritative text.

🇬🇧 English

This notice announces a virtual public meeting to discuss the Animal Drug User Fee Act (ADUFA) and invites public comments on the program and its reauthorization. Stakeholders in the animal drug industry are encouraged to participate and share their views on potential improvements or changes before the current authorization expires in 2028.

AI-generated summary. May contain errors. Refer to official sources for legal decisions.

Key Changes

  • Public meeting scheduled to discuss ADUFA's future
  • Invitation to provide comments on program reauthorization
  • FDA seeks input on potential changes to enhance ADUFA

Obligations

What this law requires

critical

The FDA must hold a public meeting to gather public input on the reauthorization of the Animal Drug User Fee Act.

FDA
May 27, 2026
operational
medium

Stakeholders in the animal drug industry must register to attend the public meeting by emailing their complete contact information by May 22, 2026.

stakeholders in the animal drug industry
May 22, 2026
operational
high

The FDA must publish comments received on its website following the public meeting.

FDA
disclosure
medium

Individuals wishing to make an oral presentation must submit their request during registration by May 1, 2026.

individuals and organizations in the animal drug industry
May 1, 2026
operational
medium

Members of the public interested in attending the public meeting must register by May 22, 2026.

members of the public
May 22, 2026
reporting

Affected Parties

Animal drug industry stakeholdersFDA

Tags

Animal health,Public meeting,Regulatory feedback