Navigating the United States Pharmacopeia (USP) is crucial for professionals in the pharmaceutical, cannabis, and herbal drug industries. Despite its importance, many find the USP difficult to interpret without prior experience. This webinar aims to demystify the USP, providing practical guidance for QA reviewers, QC chemists, new science graduates, and industry professionals.
By breaking down general chapters, product monographs, reagents, indicators, solutions, and general notices, participants will gain a comprehensive understanding of USP’s structure and application. Real-life case studies will illustrate effective documentation review, equipping attendees with the skills to navigate USP confidently and accurately.
Join us to enhance your knowledge and streamline your work processes with actionable insights from industry experts.
Who Should Attend
This webinar is designed for quality assurance reviewers, quality control chemists, science graduates, and industry professionals who work within the pharmaceutical, cannabis, and herbal drug industries. It is particularly beneficial for those responsible for ensuring product quality and compliance with USP standards. Additionally, anyone interested in gaining a deeper understanding of the USP’s structure and application will find this training invaluable for enhancing their professional expertise and effectiveness in documentation review and regulatory compliance.
Workshop Outline
Introduction to USP
Understanding the role and significance of USP in the industry
Overview of USP’s history and its evolution
General Chapters
Structure and purpose of general chapters
Key chapters relevant to various industries
Interpretation and application in daily operations
Product Monographs
Understanding monographs: structure and components
How to read and interpret monographs
Case studies on product monograph reviews
Reagents, Indicators, and Solutions
Overview of reagents, indicators, and solutions section
Key reagents and their applications
Interpretation and usage guidelines
General Notices and Requirements
Purpose and scope of general notices
Key requirements and how they affect product compliance
Case studies on applying general notices in documentation review
Case Studies
Real-world examples of documentation review
Practical tips for effective USP navigation
Interactive exercises to reinforce learning
Learning Outcomes
Comprehensive Understanding of USP:
Gain a thorough understanding of USP’s structure and components, enhancing your ability to navigate and utilize the pharmacopeia effectively.
Interpreting General Chapters and Monographs:
Develop skills to accurately interpret and apply general chapters and monographs in various industry contexts.
Review Preparations of Reagents, Indicators, and Solutions:
Learn the correct usage and interpretation of reagents, indicators, and solutions within the USP framework.
Applying General Notices and Requirements:
Understand the importance of general notices and requirements and learn how to apply them to ensure product compliance.
Case Study Mastery:
Analyze real-world documentation to reinforce understanding and application of USP guidelines, preparing you for practical industry challenges.
All participants will receive a certificate of attendance upon completion of the workshop.
Recorded Webinar – Navigating the USP: Practical Guidance for QA, QC and Industry Professionals