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American Pharmaceutical News In Review
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May 03, 2017
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» Industry News
 
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» Featured Articles
A New Risk Assessment Tool for Regulatory Starting Material Evaluation
A New Risk Assessment Tool for Regulatory Starting Material Evaluation
According to ICH Q7, a starting material is defined as the point at which the sponsor commits to GMP... read more »
Supercritical Fluid Chromatography: An Essential Tool in Drug Discovery
Supercritical Fluid Chromatography: An Essential Tool in Drug Discovery
Since its early introduction in the 1960s, Supercritical Fluid Chromatography (SFC) has had a slow ... read more »
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» Featured Announcements
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  How Polymer Science is Changing the Functional Role of Capsules
Live Webinar
Never have so many drug delivery systems based on hard capsules been available to pharmaceutical ... read more »
» Featured Video
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  Interview with SP Scientific at Interphex 2016
Interview with SP Scientific at Interphex 2016
In this video, Mike Auerbach speaks with Paul Coiteux and Kain Johnson of SP Scientific about the recent acquisition of PennTech. With this ... read more »
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  Webinar: Expert Knowledge: The Prescription for Improving Karl Fischer Titrations
Webinar: Expert Knowledge: The Prescription for Improving Karl Fischer Titrations
The quality, efficacy, and shelf life of lyophilized pharmaceutical products and ingredients depends on water content. Routine Karl Fischer titration ... read more »

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» Featured Products
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  Biopharm UNIFI System
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» Featured Whitepaper
Development and applications of novel, highly sensitive fluorescent dyes for N-glycan analysis
Development and applications of novel, highly sensitive fluorescent dyes for N-glycan analysis
Glycosylation is one of the key critical quality attributes of monoclonal antibody–based biotherapeutics. Glycosylation changes can impact a biological drug’s safety, efficacy, clearance, and ... read more »
The Use of EDX Fluorescence Spectrometry for Pharmaceutical Elemental Impurity Analysis Based on USP
The Use of EDX Fluorescence Spectrometry for Pharmaceutical Elemental Impurity Analysis Based on USP <735>
In May 2015, the United States Pharmacopeia (USP) established general chapter <735>, permitting the use of X-ray Fluorescence (XRF) Spectrometry in pharmaceutical testing for elemental impurities. Perhaps ... read more »

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| Events
EVENT
  Vibrational Spectroscopy for Pharmaceutical Applications
Webinar –  05/18/2017
This webinar will contain the latest advances in FT-IR and Raman instrumentation, and applications will be reviewed with a thorough discussion of ...
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EVENT
  Webinar: Effective Compressed Gas Contamination Monitoring: Particles and Microbials
Webinar –  05/24/2017
Control of the environment in which pharmaceutical products are manufactured is a key element of Good Manufacturing Practices (GMP). Monitoring of ...
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