Analysis of Elemental Impurities in Raleigh, NC

Sign-in will begin at 8:30. The lecture will begin promptly at 9:00.

January 9, 2013

Course Descriptions

Analysis of Elemental Impurities

This course will cover the official chapters <232> / <233> that appeared in Second Supplement to USP-NF 30 (official Dec 1, 2012) for analysis of Elemental Impurities in pharmaceutical materials. The course addresses the elements and how limits are set. It will explain how it applies to products and goes through a brief method description. Recent changes will be highlighted as well as the implementation timeframe and ICH Q3D.

Methodologies and Procedures

Explain the recent changes that occured in the Chapters [232] and [233] in the Second Supplement to USP35 and the implementation timeframe for the new requirements to become official Understand the issues associated with USP Chapter [231]--Heavy Metals that resulted in development of new proposed chapters on elemental impurities Understand the scope and context of USP's new chapters on elemental impurities Develop an understanding of how the limits are applied to products Explain proposed procedures and acceptance criteria

Who Should Participate: 

Analytical chemists, QC managers, QA managers, compliance managers, lab managers, production managers and any individual in the pharmaceutical industry with an interest in the application of ICP and ICP-MS to the analysis of metals in API's, excipients, and drug products.

Dates Offered

Cork, Ireland
1950 Kraainem, Belgium
91978 Courtaboeuf Cedex-Les Ulis, France
4310 Rheinfelden, Aargau, Switzerland
Minneapolis, MN, United States
Coral Gables, FL, United States
Irvine, CA, United States
Barcelona, Spain
Milan 20124, Lombardy , Italy

Registration Information

Regular Price Information: 

US $215


1101 Gorman Street
United States
Contact Information