Stay ahead of critical regulatory changes with this in-depth course on the DEA’s proposed revisions to quota management for schedule I and II controlled substances, including ephedrine, pseudoephedrine, and phenylpropanolamine. Learn about new quota subcategories, revised application procedures, and the expanded role of stakeholder input in shaping the final regulation. Get practical knowledge to ensure compliance, prevent diversion, and understand the supply chain visibility requirements affecting manufacturers and importers.
In this course you will learn the following:
* Understand the goals and intent behind the proposed rule.
* Identify the key regulatory changes and their implications.
* Recognize the process for public participation and comment submission.
* Describe the structure and subcategories of manufacturing and procurement quotas.
* Assess the potential impact of the proposed rule on affected entities.
* Appreciate the evolving nature of the rule based on stakeholder input.
