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July 23, 2021
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  Webinar: Understand the new FDA and EMA regulations

Watch our on-demand webinar that will provide a complete review of the recent regulatory changes on nitrosamines contamination in pharmaceuticals. We will also offer a comprehensive guide on testing best practices proposed in the USP <1469> and EP 2.5.42 chapters.

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» Industry News
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  Ligand Partner Jazz Pharmaceuticals Launches RYLAZE™
Ligand Pharmaceuticals Incorporated announced that Jazz Pharmaceuticals plc has launched Rylaze™ (... read more »
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  Akston Biosciences to Supply Seppic’s Adjuvant to Create Shelf-Stable COVID-19 Vaccine
Akston Biosciences Corporation, a developer of new classes of biologic therapeutics, announced a ... read more »
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  FDA Expands Indication for PROGRAF® for Lung Transplant Recipients
Astellas Pharma Inc. announced that the U.S. FDA approved its supplemental New Drug Application (... read more »
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  Pfizer Expands Recall to Twelve Lots of Chantix Tablets
Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots of Chantix 1 mg Tablets,... read more »

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» Infographic
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  Top 5 Tips for Easier Bacterial Endotoxin Testing (BET)
BET is an essential step of pharmaceutical manufacturing for injectable drugs and implantable medical devices. Testing for endotoxins prevents fever ... read more »
» Featured Articles
A Model for Aseptic Operations Governance (Structure, Competencies, Governance and Attitude)
Manufacturing sterile parenteral products with aseptic technique has become more complex because of multiple technical, scientific and compliance ... read more »
Drug Development in Oncology in the Era of Precision Medicine
Cancer research is complex: trials require specific design expertise and often include biomarker and companion diagnostics, and failure rates tend to ... read more »
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» Featured Video
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  On-Demand Webinar: A Straightforward Path Toward Regulatory Compliance and Data Integrity with Your Microbial Testing Systems
On-Demand Webinar: A Straightforward Path Toward Regulatory Compliance and Data Integrity with Your Microbial Testing Systems watch »
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  On-Demand Webinar: Risk Assessment for Potential Elemental Impurities on Drug Products/Medical Devices
This webinar will address how to deal with “Risk Assessment for Potential Elemental Impurities” on Drug Products and Medical Devices. The USP, in ... watch »

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» Featured Whitepaper
eBook: Good Identification Practices for Organic Extractables and Leachables Via Mass Spectrometry
An important class of drug product or medical device impurities is leachables. Leachables are foreign impurities that are present in a drug product because of its chemical interaction (leaching) with... read more »

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| Events
EVENT
  13th Annual Next Generation Dx Summit
Grand Hyatt Washington, D.C. & Online –  08/24/2021
The Next Generation Dx Summit brings together international diagnostic professionals working in the field and offers unparalleled insight from ...
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EVENT
  Microscopy & Microanalysis 2021
Virtual –  08/01/2021
Brought to you by the Microscopy Society of America (MSA) and the Microanalysis Society (MAS), the M&M conference is the largest scientific meeting ...
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