FDA Regulatory Compliance for New Animal Drugs in Animal Feeds
Stay ahead of regulatory changes with a comprehensive course on the updated FDA rules for new animal drugs in animal feeds. This training details the specific legal authorities, application types (original, conditional, supplemental), documentation, labeling, and sponsor requirements as outlined in 21 CFR Part 558 and related parts. Gain clarity on actionable compliance steps, recordkeeping obligations, and the consequences of non-compliance—empowering you to protect your business and maintain uninterrupted market access.
In this course you will learn the following:
* Identify the legal authorities governing new animal drugs for use in animal feeds.
* Understand the types of applications (original, conditional, supplemental) and their approval processes.
* Recognize the specific requirements for labeling, sponsor identification, and conditions of use.
* Implement the new or revised requirements for approved animal drugs in feed.
* Understand the consequences of non-compliance with the Final Rule.
NOTE: Unless otherwise indicated, all course purchases are for access to the course for a period of 1-year. At the end of the one year term, the course will be set to “inactive”.
