Key factors for successful compliance with USP 795
USP 795 addresses the extemporaneous compounding of non-sterile pharmaceuticals by explaining what constitutes good compounding practice and establishing guidelines that minimize the likelihood of error or cross-contamination. The Chapter has undergone multiple revisions incorporating new science and evidence-based guidance and best practices, yet the current USP 795 chapter version published in 2014 is the official standard.
However, enforcement of the Chapter standards has been inconsistent, drawing little attention from regulatory agencies and pharmacy leaders alike, while other USP compounding chapters have taken precedence. Because of these ongoing revisions and lack of regulatory scrutiny, many pharmacies have not yet developed a robust USP 795 compliance program.
In this webinar, you will:
- Gain practical steps you can take toward USP 795 compliance
- Understand key factors for successful compliance with USP 795
- Learn common pitfalls to avoid when assessing your pharmacy for USP 795 compliance