American Pharmaceutical News In Review

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February 23, 2022

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Why is HPLC-CAD the Top Method for Excipient Analyses?

Pharmaceuticals could lose significant efficacy, stability, and safety without added excipients. While conventional analytical HPLC-UV or LC-MS methods are standard formula development, these techniques fall short when the supporting additives lack a chromophore or cannot form gas-phase ions. But you can easily overcome analyte incompatibility issues using the near-universal charged aerosol detector (CAD). Download this free eBook to discover the benefits of HPLC-CAD analysis to measure excipient stability, impurities and degradation products.

	Industry News

Health Canada Authorizes Novavax's Nuvaxovid COVID-19 Vaccine
Health Canada authorized Novavax's Nuvaxovid COVID-19 vaccine for the prevention of COVID-19 in ... read more »

Sandoz Launches Generic Lenalidomide in 19 Countries Across Europe
Sandoz announced the launch of generic oncology medicine lenalidomide, indicated for several haemato... read more »

Alvea Launches Scalable, Shelf- Stable DNA Vaccine Development against New SARS-CoV-2 Variants
Alvea will begin to develop, test, and deliver DNA vaccines at scale to low and middle-income ... read more »

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 »

	Infographic

Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Recombinant Horseshoe Crab Factor C (rFC) provides a sustainable, highly effective, and environmentally friendly sustainable means of endotoxin ... read more »

	Featured Articles

An Interview with Renee Morley, MBA Contec. Inc. is an experienced global leader in wipers, mops, and disinfectants for the pharmaceutical industry. Contec focuses on providing the ... read more »

Changing the Methods Used for Inactivation of Microorganisms and Viruses For many years pharmaceutical companies have relied upon chemical methods to inactivate microorganisms and viruses present in their facilities. Over ... read more »

	Featured Video

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 »

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 »

	Featured Products

4Cell® Nutri-T Medium
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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 »

	Events

Drug Discovery Chemistry
Hilton Bayfront – 04/18/2022
Focused on discovery and optimization challenges of small molecule drug candidates, Drug Discovery Chemistry is a dynamic in-person and online event ... event details »

PDA Pharmaceutical Microbiology Conference
Washington, DC – 10/10/2022
The 2022 PDA Pharmaceutical Microbiology Conference continues the ongoing tradition of addressing the most relevant opportunities and challenges to ... event details »

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