Understanding & Implementing New USP Chapters for Pharmaceutical Analysis and Instrument Qualification. Industry experts, including Dr. Ludwig Huber from LabCompliance.com, and Agilent Technologies have developed a new series of USP e-seminars, tailored to the needs of quality managers and analysts working in drug development and manufacturing QA/QC.
This e-seminar series offers you a convenient way to stay up to speed with current and adapted USP regulations.
There are no live events at this time.
For e-Seminars related to a specific industry, see:
Recorded Events - Attend at Your Convenience
Title
Residual Solvent Analysis According to USP <467> -Understanding and Implementing the new chapter.
A Replacement for USP 231 Heavy Metals using ICP-MS. Improve Accuracy and Productivity using ICP-MS for the Measurement of Heavy Metals in Pharmaceutical Materials.
Improve Compliance with Regulatory Requirements for e-Records, Faster Result Review with an Enterprise Content Management System.
USP 467 - Adapting to the New RequirementsDownload Slide Set
Understanding and Implementing USP Chapter <1058> for Analytical Instrument Qualification in your Laboratory