American Pharmaceutical News In Review

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February 25, 2022

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Register Now: Pros and Cons of a Dedicated Cleanroom Monitoring System

This webinar will describe the basic concept of a dedicated pharmaceutical cleanroom monitoring system (FMS) in comparison with other, multi-application systems such as Building Management Systems (BMS), with clear pros and cons.

Differences between computer-based and industrial designed FMS will be discussed, with a focus on system reliability and data integrity aspects.

	Industry News

Novavax Announces Shipments of its COVID-19 Vaccine to European Union Member States
Novavax, Inc. announced the first doses of Nuvaxovid™ COVID-19 Vaccine (recombinant, adjuvanted) ... read more »

MilliporeSigma Announces Closing of Exelead Acquisition and Plans to Invest More Than € 500 Million in Technology Scale-Up
MilliporeSigma announced the closing of the transaction to acquire Exelead, following regulatory ... read more »

Alvotech and Fuji Pharma Expand Partnership for Additional Biosimilar Candidate in Japan
Alvotech Holdings S.A. and Fuji Pharma have agreed to add to their strategic partnership for the ... read more »

Moderna and Thermo Fisher Scientific Announce Long-Term Strategic Collaboration
Moderna, Inc. and Thermo Fisher Scientific Inc. announced a 15-year strategic collaboration ... read more »

	Infographic

Make the Switch to Automated At-line Testing for Mycoplasma: Four compelling reasons to upgrade now
Make the Switch to Automated At-line Testing for Mycoplasma
Fully automated PCR systems have been introduced into the market and offer several improvements over traditional PCR-based methods and can be used to ... read more »

	Featured Articles

Functional Challenges for Alternative Bacterial Endotoxins Tests Part 4: Beyond Recombinant Reagents Introduction The two compendial tests, <151>, “Pyrogen Test” and <85>, “Bacterial Endotoxins Test” (henceforth “RPT” and “BET” respectively) share a common reason for their... read more »

Key CMC Considerations for Biologic Development Taking a new biologic therapeutic from a research bench to the market is a cumbersome process. Like small molecule drugs, biologics must be approved ... read more »

	Featured Video

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 »

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 »

	Featured Products

PURELAB® Chorus 1 Complete Ultrapure Water System
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	Featured Whitepaper

Microbiological Quality of Non-sterile Products: Culture Media for Compendial Methods
High quality harmonized USP <61> & <62> compliant media is key to successful non-sterile release and incoming testing of materials that need to be free of specified and objectionable microorganisms. Download ... read more »

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

Pittcon Conference and Expo
Georgia World Congress Center – 03/05/2022
Pittcon is a friendly, welcoming environment where analytical chemists at all professional levels meet. Pittcon is a platform for sharing ideas and ... event details »

INTERPHEX 2022
Javits Center, NYC – 05/24/2022
INTERPHEX is the premier pharmaceutical, biotechnology, and medical device development and manufacturing event where you can “Experience Science ... event details »

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