Analysis of Elemental Impurities in Raleigh, NC

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

Classroom
January 9, 2013

Course Descriptions

Analysis of Elemental Impurities

This course will cover the revisions of 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.

Category: 
Methodologies and Procedures
Objectives: 

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

June 5, 2013
Cork, Ireland
July 8, 2013
1950 Kraainem, Belgium
July 9, 2013
91978 Courtaboeuf Cedex-Les Ulis, France
July 11, 2013
4310 Rheinfelden, Aargau, Switzerland
July 18, 2013
Minneapolis, MN, United States

Registration Information

Regular Price Information: 

US $215

Venue

McKimmon Center
1101 Gorman Street
Raleigh
NC
United States
919-515-2277
Contact Information
pharmed@usp.org
301-230-6304