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February 27, 2023

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Release and Stability Testing for Parenteral Drug Products
Sponsored by Nelson Labs
Release and stability testing are a vital part of new drug development and are conducted throughout a product’s life cycle. They are studies that confirm the quality, safety, and efficacy of a drug product throughout that product’s shelf life. Learn how and why release and stability testing are critical for parenterals.

	Industry News

AskBio Receives European Orphan Drug Designation Through BrainVectis for AB-1003, An Investigational AAV Gene Therapy to Treat Muscular Dystrophy
AskBio, a subsidiary of Bayer AG, has announced that its gene therapy AB-1003 (also known as LION-... read more »

FDA Authorizes First OTC At-Home Test to Detect Both Influenza and COVID-19 Viruses
The FDA has granted emergency use authorization for the first at-home diagnostic test that can ... read more »

Dr. Reddy's Laboratories to Acquire Mayne Pharma’s U.S. Generic Prescription Product Portfolio
Dr. Reddy's Laboratories has agreed to purchase Mayne Pharma Group's U.S. generic prescription ... read more »

AstraZeneca Completes Acquisition of CinCor Pharma
AstraZeneca has successfully acquired CinCor Pharma, a clinical-stage biopharmaceutical company ... read more »

	QC Corner

Effective Contamination Control Strategy and Microbial ID Workshop
What is an effective contamination control strategy, microbial ID methodology? This video goes in-... read more »

	Infographic

Biopharmaceutical Characterization: Evaluation Criteria to Help You Choose the Right Partner
This infographic looks at a number of points to consider when choosing your contract research organization partner. read more »

	Featured Articles

		Cleaning, Disinfection and the Problems Caused by Chemical Residues Cleaning and disinfection are necessary protective and reactive steps to address microbial deposition on surfaces within pharmaceutical cleanrooms. An... read more »

		The Lifecycle from Drug Development Through Approval Processes The average lifecycle of drug development from discovery to approval is about 10 to 12 years. The total time varies depending on the previous ... read more »

	Featured Video

On-Demand Webinar: How to Overcome Barriers in Raw Material Identification
In this live webinar, hear from Soleil Grise and Chris Welsby, from Agilent, as they discuss how to overcome barriers in raw material identification. watch »

On-Demand Webinar: Lower Bioprocessing Costs and Time with Raman Spectroscopy
In this live webinar, hear from Dean Stuart as he talks about Lower Bioprocessing Costs and Time with Raman Spectroscopy watch »

	Featured Products

Labrasol® ALF
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Transcutol® HP
Gattefossé Diethylene glycol monoethyl ether NF/EP (>99.9% purity) learn more »

Labrafac™ MC60
Gattefossé Glyceryl mono and dicaprylocaprate NF / Glycerol monocaprylocaprate (Type I) EP learn more »

	Featured Whitepaper

eBook: Surface Analysis Utilizing Infrared and Raman Microscopy
In this eBook we cover reverse engineering of materials and polymers, depth profiling of complex samples, and other analysis and applications of raman microscopy. read more »

App Note: Preparation of Standards For Chromatographic Analysis
In analytical R&D or QA/QC laboratories, accurate standard preparation is crucial for the quality of the analytical results, which in turn has an enormous effect on laboratory efficiency. This ... read more »

	More Products

AdvaTab Orally Disintegrating Tablet Technology Learn More
CELPHERE MCC Spherical Seed Core Learn More
PF22 Tabletop Aseptic Filler Learn More

	Directory Categories

Excipient Search Search More

Microbial Detection Systems Search More

Capsule Filling Equipment Search More

	Events

DCAT Week
New York, NY – 03/20/2023
The Premiere Event for the Global Bio/Pharmaceutical Manufacturing Value Chain event details »

Drug Discovery Chemistry
San Diego, CA – 04/10/2023
Drug Discovery Chemistry is a dynamic conference for medicinal and biophysical chemists working in pharma, biotech, and academia. Focused on discovery... event details »

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