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January 04, 2017
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» Industry News
 
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» Featured Articles
An Interview With... Aileen Ruff VP, Business Unit Strategy and Marketing, Drug Delivery Solutions, Catalent
An Interview With... Aileen Ruff VP, Business Unit Strategy and Marketing, Drug Delivery Solutions, Catalent
The Pharmatek acquisition brings spray drying into Catalent’s portfolio of drug development ... read more »
An Interview With... Holly Haughney, PhD, Pall Life Sciences
An Interview With... Holly Haughney, PhD, Pall Life Sciences
Small molecule drug manufacturers have been applying semi-continuous processes with success for some... read more »
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» Featured Announcements
14th Annual Biopharmaceutical Manufacturing Report and Survey.
14th Annual Biopharmaceutical Manufacturing Report and Survey.
Participate in the bio-industry's most in-depth, global benchmarking and analysis study: 14th Annual... read more »
» Featured Video
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  Webinar: New Intrinsically Enteric Capsule Technology for Pharmaceutical Drug Development
Webinar: New Intrinsically Enteric Capsule Technology for Pharmaceutical Drug Development
Finding more efficient ways to target drug delivery to the small intestine and provide effective enteric protection for heat or acid-sensitive and/or ... read more »
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  Webinar: Enabling custom solutions for downstream processing for future therapies
Webinar: Enabling custom solutions for downstream processing for future therapies
In this webinar, we will discuss resin prototype development, optimization of key parameters such as surface and immobilization chemistry, ligand ... read more »

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» Featured Products
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  Gemini HPLC Columns
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» Featured Whitepaper
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 »
Through-Container ID Verification of Polysorbates 20, 40, 60 & 80 with RapID
Through-Container ID Verification of Polysorbates 20, 40, 60 & 80 with RapID
Polysorbates are often packaged in a sealed, oxygen-free environment to prevent degradation. Amber glass bottles are common containers for polysorbates, often used in large numbers, which makes ... read more »

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| Events
EVENT
  IFPAC®-2017
North Bethesda, Maryland (Washington, D.C.) U.S.A. –  02/27/2017
Advanced Manufacturing Science… Emerging Technologies to Modernize Pharmaceutical/Biopharmaceutical Development and Manufacturing IFPAC is the ...
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EVENT
  Pittcon 2017
McCormick Place –  03/05/2017
Pittcon, the world’s leading annual conference and exposition for laboratory science, shines light on new technology and scientific research. ...
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