Evolution of USP<1058> updates and insights in regulations
The United States Pharmacopeia (USP) is the only major pharmacopeia with a general chapter dedicated to analytical instrument qualification (USP <1058>). This makes <1058> a globally significant regulatory reference. However, despite the significant changes with the 2017 edition of <1058>, 68% of laboratories have not updated their qualification procedures. Additionally, the USP has already started the process to initiate updates to <1058>, when many laboratories may not fully comply with the current edition!
This raises many questions about the role of the current <1058> general chapter and how it aligns with the recently issued 2nd Edition of GAMP® 5.
By attending this webinar you will learn about:
- How USP <1058> aligns with GAMP® 5
- Core elements of the <1058> instrument life-cycle framework
- Areas of <1058> the USP are exploring improvements in
Presenter: Paul Smith (Global Laboratory Compliance Marketing Specialist (USP <1058>), Agilent Technologies, Inc.)
Paul has a passion for laboratory compliance and started his career as an Infrared Spectroscopist, performing his first FT-IR software validation in 1992, 30 years ago. In his current Agilent role, Paul is an active member of GAMP, a member of the UK GAMP Community of Practice (CoP) steering committee and has contributed to GAMP® Good Practice Guides. He helps laboratories understand their laboratory instrument qualification requirements and writes publications and white papers about this.
