Irvine Pharmaceutical Services
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  A Pharmaceutical Development Company

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