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February 19, 2015
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  Using USP 735 As An Alternative to USP 232/233 for Elemental Impurity Analysis in Pharmaceutical Products
From Shimadzu
With new USP regulations for elemental impurity analysis becoming enforceable in late 2015, many laboratories are getting prepared to fulfil these requirements. This webinar will discuss one alternative approach to elemental impurity analysis that meets the requirements of sensitivity and repeatability with very little sample preparation.

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» Industry News
 
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» Featured Articles
HORIZON LINES: A Quarterly Review of NDAs
HORIZON LINES: A Quarterly Review of NDAs
New Drug Application (NDA) approval involves various steps including pre-clinical research, investigational new drug application, clinical studies, and NDA review. NDAs can be obtained for new ... read more »
Supply Chain Guidance and the United States Pharmacopeia Direction
Supply Chain Guidance and the United States Pharmacopeia Direction
The ongoing health care crisis around drug safety and reliability has the attention of the global regulatory agencies responsible for providing the public with safe health care products. Regulatory ... read more »
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» Featured Partners
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  Benefit from 50 years of CMO knowledge
From Ash Stevens
Benefit from 50 years of CMO knowledge, visit ashstevens.com and contact Ash Stevens today. read more »
» Featured Video
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  Webinar: The Role of the Monitor: Considerations to Adopting a Risk-Based Monitoring System
Webinar: The Role of the Monitor: Considerations to Adopting a Risk-Based Monitoring System
Marcus Thornton, Senior Director of Medidata Solutions, discusses considerations to adopting a risk-based monitoring system. read more »

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» Events
 
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