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American Pharmaceutical News In Review
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March 14, 2022
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  Confused about choosing a chromatography method? Turn to the molecules for answers.

Struggling to make sense of the growing number of chromatography options? Our blog helps you focus on what’s most important — the molecular attributes of your sample. Learn how specific properties can guide your chromatography strategy to maximize yield and improve efficiency.?? Read the blog now to take the guesswork out of your chromatography strategy.

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» Industry News
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  Servier Submits Marketing Authorization Application to EMA for TIBSOVO®
Servier has submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (... read more »
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  Genetic Leap and Astellas Establish Research Collaboration to Develop RNA-targeted Small Molecules for Oncology Target
Genetic Leap announced a research collaboration agreement with Astellas Pharma, Inc. to develop ... read more »
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  UCB Acquires Zogenix
UCB acquired Zogenix for US$ 26.00 per share plus a potential cash payment of $ 2.00 per share. The ... read more »
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  The Bioindustry's Most In-Depth, Global Benchmarking and Analysis Study
Your input is important as we benchmark current global and regional trends affecting the bioindustry... read more »

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» Infographic
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  5 Reasons to Switch to Multi-Column Chromatography
5 Reasons to Switch to Multi-Column Chromatography
Multi-column chromatography (MCC) technologies can transform existing batch processes and provide many advantages such as up to 80% reduction in ... read more »
» Featured Articles
Data Integrity in the QC Lab – Reducing the Potential for Human Error in Endotoxin Testing
Data integrity is of the utmost importance when testing and analyzing products and devices in the Quality Control (QC) laboratory. In an increasingly ... read more »
FDA Withdrawal of Temporary COVID-19 Pandemic Hand Sanitizer Manufacturing Guidelines; Additional Testing May Be Required
All hand sanitizers, whether used by consumers or healthcare professionals, are considered over-the-counter (OTC) drugs that are regulated by the FDA.... read more »
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» Featured Video
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  On-Demand Webinar: Viral Control in Pharmaceutical Processing
This webinar discusses the essential elements of control, testing, and remediation and it includes a spotlight on the maim viruses of concern. watch »
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  On-Demand Webinar: Microbial Identification in a Manufacturing Environment
In this webinar we will discuss how recent technological developments allow for rapid micro testing and rapid micro identification, focusing on the ... watch »

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» Featured Products
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  Luminata Product Development Software
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» Featured Whitepaper
eBook: Key Learnings in Mycoplasma Detection for Biologics Quality Control
It is important for the safety and purity of biological products to assure that cell substrates and unprocessed bulk material used during manufacture are free of mycoplasmas. Additionally, regulatory ... read more »
eBook: Analytical Method and QC Testing Strategies for Biologics Production
Development of a manufacturing process for a biotherapeutic that ensures consistent quality, purity and safety is a critical step in successfully developing the drug, getting it approved by regulatory... read more »

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| Events
EVENT
  SMi’s 6th Annual Highly Potent Active Pharmaceutical Ingredients
London, UK –  05/09/2022
The Global High Potency API/HPAPI Market is projected to reach 37 billion USD by 2027, growing at an ever-increasing CAGR of 8.43%. The expanding ...
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EVENT
  IFPAC 2022
North Bethesda, MD –  06/12/2022
IFPAC brings together experienced professionals and the next generation of leaders to share in discussions, give input and get ideas for the future ...
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