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April 19, 2022

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Ensuring Drug Safety through Sterilization of Parenteral Products and Evaluation of Extractables

How do you help ensure that your pharmaceutical product can be released to market as quickly and safely as possible? Some important things you must consider include regulatory expectations, container closure integrity, extractables and leachables, method validation, and sterilization assurance. You can learn directly from our industry experts in Philadelphia on May 11th and 12th. There will be two days full of information and discussion about sterilization and lab testing. Learn more.

	Industry News

FDA Authorizes First COVID-19 Diagnostic Test Using Breath Samples
The U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first ... read more »

Nektar and BMS to End Clinical Development Program for Bempegaldesleukin in Combination with Opdivo
Nektar Therapeutics and Bristol Myers Squibb announced that based on results from pre-planned ... 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 »

Health Canada Approves KEYTRUDA® for Adult Patients with High-Risk Early-Stage Triple-Negative Breast Cancer
Merck announced that Health Canada has granted approval for KEYTRUDA® (pembrolizumab), Merck's anti-... read more »

	QC Corner

QC Corner: Environmental Monitoring as a Component of a Contamination Control Strategy
Watch Now! In this webinar, Mark Hallworth discusses environmental monitoring as a component of a ... read more »

	Infographic

Reducing Risk in Drug Development
Reducing Risk in Drug Development
Proactive microbial detection using real-time Total Organic Carbon (TOC) and Conductivity technologies offer better process control and can mitigate ... read more »

	Featured Articles

Current Updates on In-vitro Drug Release Testing of Long-Acting Injectables Long acting injectables (LAIs) are drug products, intended for administration through the parenteral route and designed to release Active ... read more »

Event-Based Sterility Assurance Event-related sterility assurance is, simply put, any event that compromises the integrity of the barrier enclosing the sterilized material. Such ... read more »

	Featured Video

On-Demand Webinar: Back to Basics: Growth Promotion Testing
In this webinar you’ll learn the rules for performing growth promotion testing, why we perform growth promotion testing and best practices. watch »

On-Demand Webinar: Sophisticated Formulation Approaches for Insoluble Drug Candidates
The webinar will explain the role nano-formulations play to accelerate the drug discovery/development process. It will also outline a formulation ... watch »

	Featured Products

Plasdone™ K-90 PVP
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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 »

Whitepaper: Comprehensive Pure Water Guide for Pharmaceutical Engineers
In today’s pharmaceutical facilities the availability of purified water is essential. While the domestic consumer considers tap water to be “pure”, the pharmaceutical end-user regards it as grossly ... read more »

	Events

PREP 2022: 35th International Symposium and Exhibit on Preparative and Process Chromatography
Baltimore Inner Harbor, MD – 05/15/2022
The program is packed with papers on biochromatography, downstream processing, QbD, monoclonal antibodies, plasmids, enzymes, vaccines, viral vectors ... event details »

SMi’s 9th Annual Conference Pre-Filled Syringes East Coast
Boston, MA – 04/25/2022
The global pre-filled syringes market was valued at $1139.6 million in 2020 and with the rapid growth of the industry, is expected to grow at a CAGR ... event details »

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