This webinar will provide insight into some of the hottest topics at USP which will have the greatest impact on pharmaceutical laboratories. It will provide a comprehensive overview of the major changes in the USP that have been proposed or implemented in the last year and describe strategies for keeping abreast of coming changes and how you can influence them.
This webinar will detail some of the areas with the most significant changes, and provide strategies for anticipating future changes.
Why Should You Attend:
The United States Pharmacopeia (USP) is changing more rapidly than ever - are you keeping up? You need to be aware of the pending changes especially since USP is the standard-setting organization for the FDA with expectations that you will be in compliance.This webinar will detail some of the areas with the most significant changes, and provide strategies for anticipating future changes.
Areas Covered in the Webinar:
Hot topics at USP
- Analytical procedures: Validation, verification and transfer being replaced with method lifecycle
- Weighing on an analytical balance: General Chapters < 41> and < 1251>
- Elemental impurities: Major changes are coming, but the timing and limits are uncertain
Overview of proposed or recently implemented changes
- Analytical procedures
- Basic lab tests
- Impurities
- Spectroscopy
- Dosage forms
- Packaging
- Dietary supplements
How to anticipate or influence changes
- Pharmacopeial Forum
- You opinions are important!
- Questions and discussion
Who Will Benefit:
- Quality Control Personnel
- R&D Scientists in Pharmaceutical, Generic or Contract Lab Organizations
- Laboratory Supervisors and Managers
- Quality Assurance Personnel
- GMP Auditors
- CMC or Regulatory Affairs Personnel
Course Provider
Gregory Martin,
