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USP UPDATES
With heavy involvement with the United States Pharmacopeia, Irvine offers up-to-date news and events.
GMP / Auditing in Pharmaceutical Industries, December 4–5, 2008
Agenda
Registration Form
Implementation of the Residual Solvents Requirement
Responding to FDA-483 Observations
How FDA Determines Who to Hold Accountable for Violations
DEVIATION INVESTIGATIONS
USP Residual Solvents, Glycerin Monograph, and More!
Winning Inspections
AOAC Meeting Agenda
Lessons to be learned from recent scandals: FDA cannot do anything.
USP Course, TLC for Dietary Supplements: Botanicals, November 5–6, 2008
USP Compendial Discussion Group Presentations, August 1, 2008
Modified Light Obscuration, Method of Subvisible Particle, Quantification of Protein Therapeutics
Current USP Approaches to Biologics Issues
Interpretation of the New USP General Chapter <467> Residual Solvents
Pharmacopeial Monographs for Biotechnology Products
USP/FDA Joint Two-Day Regulatory & Compliance Conference, April 24 – 25, 2008
Agenda
Registration Form
USP Annual Scientific Meeting, September 24–26, 2008
New USP/FDA Guidelines effective July 1, 2008
Determining Particulate Matter Product Sheet, April 16, 2008 & June 10, 2008
USP WCDG Agenda, March 7, 2008
Residual Solvents: Results in Practice – 1 Day Seminar, February 27, 2008
Validation of Compendial Procedures,
One–Day Training Course,
January 25, 2008