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On December 1, 2019, the U.S. Pharmacopeial Convention’s (USP) Chapter <800> will become fully enforceable by regulators. This chapter addresses the physical environment and equipment needed to maintain sterility and protect the 8 million healthcare workers potentially exposed to hazardous vapors and particles each year. USP <800> is expected to be adopted by many regulators and accreditors, such as state pharmacy boards and The Joint Commission.

Join expert speaker Patricia C. Kienle, RPh, MPA, FASHP, for this 90-minute webinar, as she dives into the different types of hazardous drugs and the requirements for compliance.

Here's a look at the webinar agenda:

Regulatory and accreditation status of USP <797> and <800>
- What organizations expect regarding USP compliance
- Preparing for the new chapter
To whom <800> applies and in what settings
List of hazardous drugs based on the NIOSH documents
- Compiling the documents to make your list
Facility requirements
- Adapting the physical environment
Work practices
- Assessment of Risk
Safe policies and procedures
- Protecting those transporting hazardous materials
- Protecting those mixing hazardous materials
Live Q&A

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