P-Listed Hazardous Waste

P-listed waste, or “acutely toxic” waste, is formally defined by the EPA as “pure and commercial grade formulations of certain unused chemicals that are being disposed.”  To meet this definition, the unused chemical must be listed under 40 CFR 261.33 and be part of a commercial chemical product, such as a medication.

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USP <800> Compliant Hazardous Drug Spill Control Kits from Sharps Compliance

Beginning December 1, 2019, compounding pharmacies and other healthcare facilities that handle hazardous drugs (HD) must have USP <800> compliant spill kits on-site. This is an effort to protect workers in the event of accidental spills of HDs. The requirement is part of USP General Chapter 800, which “describes the practice and quality standards for handling hazardous drugs.”  Sharps Compliance is introducing the Hazardous Drug Spill Control Kit™ for the safe cleanup and disposal of spilled chemotherapy and other hazardous drugs.

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EPA’s New Pharmaceutical Rule – Origin and Reason for the Rule

The Environmental Protection Agency’s (EPA) long-awaited final rule for managing hazardous waste pharmaceuticals generated by healthcare facilities was finalized and published in the Federal Register on February 22, 2019. This rule had its origins in the EPA’s 2008 Universal Waste proposal for pharmaceutical waste – and perhaps even earlier based on comments to the EPA from retailers.

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New EPA Generator Rule Part Four: Revisions that Apply to Very Small Quantity Generators

The new rule changed the name of the Generator Classification for those persons that produce the least amount of waste from Conditionally Exempt Small Quantity Generator to Very Small Quantity Generator. There are Limited Requirements under both the previous regulations and the new final rule.
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