Watch compounding expert, Eric S. Kastango, BS Pharm, MBA, FASHP, in a webinar as he discusses best practices for USP <795> compliance.
Pharmacies compounding nonsterile medications have been required to follow USP 795 requirements since 2000. For the last twenty years, the chapter has undergone multiple revisions incorporating new science and evidence-based guidance and best practices, which lead us up to the most recent revision on June 1, 2019.
While currently under appeal, once the appeals process is complete, the 2019 version will become official and enforceable by regulatory (state boards of pharmacy and FDA) and accreditation agencies, (Joint Commission and PCAB). Learn more about key areas of focus and best practices for USP 795 compliance.
At the conclusion of this webinar, you will be able to understand:
- Key areas of focus and best practices to ensure compliance with USP 795
- Notable changes to the 2019 version of USP 795 including the requirements of Policies and Procedures (P&Ps), a dedicated person, master formulation and daily documentation
- What we know about the appeals process for USP 795 and 797