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American Pharmaceutical News In Review
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May 12, 2017
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   Live webinar: Effective Compressed Gas Contamination Monitoring: Particles and Microbials- Register now

Control of the environment in which pharmaceutical products are manufactured is a key element of Good Manufacturing Practices (GMP). Monitoring of particles and microorganisms in manufacturing cleanrooms, Restricted-Access Barrier Systems (RABS), and isolators consists of clearly defined components.

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» Industry News
 
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» Featured Articles
Alternative Strategies to Reversed-Phase Liquid Chromatography for the Analysis of Pharmaceutical Compounds
Alternative Strategies to Reversed-Phase Liquid Chromatography for the Analysis of Pharmaceutical Compounds
Reversed phase liquid chromatography (RPLC) is the gold standard analytical strategy in the ... read more »
An Interview With... Heidi Heck, Director, Analytical Development, Nitto Denko Avecia Inc.
An Interview With... Heidi Heck, Director, Analytical Development, Nitto Denko Avecia Inc.
Avecia manufactures custom-synthesized oligonucleotide drug substances of which the majority are ... read more »
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» Featured Video
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  Webinar: Good Manufacturing Practices for Aseptic Filling of Biopharmaceuticals
Webinar: Good Manufacturing Practices for Aseptic Filling of Biopharmaceuticals
Sterilization is a critical process that packaging components undergo when processed via aseptic conditions. There are various sterilization processes... read more »
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  Webinar: Use of TOC Analysis for Cleaning Validation and Faster Turnaround of Production Equipment
Webinar: Use of TOC Analysis for Cleaning Validation and Faster Turnaround of Production Equipment
This webinar will discuss the process and benefits of implementing Total Organic Carbon (TOC) in place of HPLC for cleaning validation through the ... read more »

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» Featured Products
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  Soluplus
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» Featured Whitepaper
Dosage Form Optimization: Technology to Advance the Patient-Centric Drug-Development Process
Dosage Form Optimization: Technology to Advance the Patient-Centric Drug-Development Process
Developing a new drug is fraught with risk. Patient-centric drug development is both a tool and a trend for drug development. By designing products with the patient in mind from the beginning of the ... read more »
Physical, Chemical, and Performance Assessment of Amorphous Solid Dispersions of Ritonavir Prepared by Hot Melt Extrusion
Physical, Chemical, and Performance Assessment of Amorphous Solid Dispersions of Ritonavir Prepared by Hot Melt Extrusion
In this study amorphous solid dispersions of ritonavir (RTV) were prepared by hot melt extrusion using the polymeric carriers AFFINISOL™ HPMC HME and copovidone at 3 different drug loads (25%, 33% and... read more »

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| Events
EVENT
  DCAT Sharp Sourcing 2017
New Brunswick, NJ –  06/27/2017
DCAT Sharp Sourcing 2017 is a conference and networking event that provides peer and customer insight on the best practices and practical ways for ... event details »
EVENT
  Webinar: Harnessing Emerging Technologies to Obtain the Best Chemical Information from Pharmaceutical Products
Webinar –  06/08/2017
Webinar: Harnessing Emerging Technologies to Obtain the Best Chemical Information from Pharmaceutical Products event details »

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