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February 05, 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
Analytical Methods and Control Strategies: The Forgotten Interface?
Analytical Methods and Control Strategies: The Forgotten Interface?
There is considerable interest in enhancing approaches for analytical method development, validation, and lifecycle management which are aligned with Quality by Design (QbD) approaches to drug ... read more »
Identifying Segmentation within the Pharmaceutical Outsourcing Market
Identifying Segmentation within the Pharmaceutical Outsourcing Market
Understanding segmentation within your market offers a variety of benefits for the forward-thinking company. Market segmentation is defined as the process of defining and subdividing a large ... read more »
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» Featured Partners
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  When you think equipment, think Federal Equipment
From Federal Equipment
Contact Federal Equipment for more information on how we can help with your equipment needs. 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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