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January 13, 2017
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  Live 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. Attend this webinar to learn about techniques and reagent considerations when testing pharmaceutical samples for moisture, and how to properly use standards to greatly improve the repeatability and accuracy of Karl Fischer titrations.

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» Industry News
 
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» Featured Articles
Controlling the Stability of Medicinal Suspensions
Controlling the Stability of Medicinal Suspensions
Many medicines in routine use are particulate suspensions of an active pharmaceutical ingredient in ... read more »
Orally Disintegrating Tablets: A Dosage Form Designed for Difficult Patient Populations
Orally Disintegrating Tablets: A Dosage Form Designed for Difficult Patient Populations
There are many patients for whom traditional tablets and capsules are not ideal dosage forms. It is ... 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: Getting the Most out of Your Standard Curve
Webinar: Getting the Most out of Your Standard Curve
The first part of this webinar will outline controls that a laboratory should consider to assure consistency in standard curves and thereby increase ... read more »
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  Webinar: API in Capsule: A Smart Approach for Rapid Drug Development
Webinar: API in Capsule: A Smart Approach for Rapid Drug Development
Micro-dosing is the procedure of dispensing precise amounts of drug substance into capsules (powder-in-capsule or PIC). The PIC approach can help on ... read more »

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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
  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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