Animal Drug and Animal Generic Drug User Fee Amendments of 2018
TITLE I--FEES RELATING TO ANIMAL DRUGS
This bill addresses the authority of the Food and Drug Administration (FDA) to collect new animal drug (brand name animal drug) and generic animal drug user fees.
Animal Drug User Fee Amendments of 2018
(Sec. 103) The bill amends the Federal Food, Drug, and Cosmetic Act to reauthorize through FY2023 the authority of the FDA to collect and use brand name animal drug user fees.
The FDA must not collect fees for (1) supplemental applications that are submitted solely to add the animal drug application number to the label of the drug, and (2) applications for genetically engineered animals that are intended to produce human medical products.
The bill revises the total amount of revenue brand name animal drug user fees can generate.
The bill also revises the requirements for calculating adjustments to revenue amounts based on changes in the workload for reviewing brand name animal drug applications.
(Sec. 104) The bill extends requirements for the FDA to report to Congress on achieving goals related to the animal drug development and review processes and implementation of the authority to collect brand name animal drug user fees.
(Sec. 107) The bill terminates the authority of the FDA to collect brand name animal drug user fees on October 1, 2023.
TITLE II--FEES RELATING TO GENERIC ANIMAL DRUGS
Animal Generic Drug User Fee Amendments of 2018
(Sec. 202) The bill reauthorizes through FY2023 the authority of the FDA to collect and use generic animal drug user fees. The FDA must not collect fees for supplemental abbreviated applications that are submitted solely to add the generic animal drug application number to the label of the drug.
The bill revises the total amount of revenue each type of generic animal drug user fee must generate.
The bill also revises the requirements for calculating adjustments to revenue amounts based on changes in the workload for reviewing generic animal drug applications.
(Sec. 203) The bill extends requirements for the FDA to report to Congress on achieving goals related to the generic animal drug development and review process and the implementation of the authority to collect generic animal drug fees.
(Sec. 206) The bill terminates the authority of the FDA to collect generic animal drug user fees on October 1, 2023.
TITLE III--MISCELLANEOUS PROVISIONS
(Sec. 301) Brand name and generic animal drug applications must be submitted electronically beginning in FY2019. Additionally, applications for conditional approval of brand name animal drugs for minor use and minor species must be submitted electronically beginning in FY2019. (Minor use drugs are for intended uses in major species [horses, dogs, cats, cattle, pigs, turkeys, and chickens] for diseases that occur infrequently or in limited geographic areas and in only a small number of animals annually.)
(Sec. 302) Product labeling for certain unapproved brand name animal drugs for minor species must include the index number in order to be marketed.
(Sec. 303) The bill prohibits the sale of brand name animal drugs that do not include the FDA application number.
(Sec. 304) The bill authorizes the FDA to grant conditional approval of a brand name animal drug not intended for a minor use or minor species if (1) the drug is intended to treat a serious or life-threatening disease or condition or addresses an unmet animal or human health need, and (2) the FDA determines that a demonstration of effectiveness of the drug would require a complex or particularly difficult study or studies.
The FDA must issue guidance or regulations that provide further details regarding the criteria for conditional approval.
The bill terminates this conditional approval authority on October 1, 2028.
The Government Accountability Office must study the effects of the conditional approval pathway for brand name animal drugs.
(Sec. 305) The FDA must issue guidance on how to evaluate certain elements of investigations as part of the animal drug application process, and how drug sponsors may obtain feedback from the agency on technical issues before submitting an application.
(Sec. 306) The FDA must review investigations conducted in foreign countries when acting on a petition for a food additive intended for use in animal food.
The FDA must also issue guidance on the voluntary pre-petition consultation process for such food additives.