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October 01, 2021
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  Designing & Qualifying LVP Packaging for Patients

As the patient need for large-volume parenterals (LVPs) increases, so does the need to design and qualify more complex LVP packaging that will contain different solutions. Assessing risk for extractables and leachables in LVP packaging at an early stage of a product’s life cycle, especially when selecting appropriate packaging material, will help ensure patient safety and product compliance. Watch our on-demand webinar to learn more.

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» Industry News
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  CVS Health Announces Availability of Pfizer-BioNTech Booster Shot to Eligible Populations
CVS Health announced that, following approval from the Centers for Disease Control and Prevention (... read more »
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  CDC Foundation Launches COVID-19 and Influenza Vaccine Resource Hub
The CDC Foundation is announcing the launch of its new Vaccine Resource Hub—an online platform that ... read more »
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  FDA Accepts Libtayo® for Priority Review for Advanced Cervical Cancer
Regeneron Pharmaceuticals announced that the FDA has accepted for priority review the supplemental ... read more »
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  Merck to Acquire Acceleron Pharma
Merck, a publicly traded biopharmaceutical company, announced that the companies have entered into a... read more »

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» Infographic
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  Measuring Total Organic Carbon (TOC) Continuously in Real-Time
Total Organic Carbon (TOC) control is essential in the production of high purity pharmaceutical water. Whether you are upgrading your current system ... read more »
» Featured Articles
Countering Misinformation Spread About the COVID-19 Pandemic
Today it’s a free-for-all on social media, which has become the main source of information for people on the COVID-19 pandemic, and sometimes a major ... read more »
QC Corner: Recent Updates to Guidances Help Standardize Extractables and Leachables Testing
Risk assessment for extractables and leachables (E&L) contained in polymeric manufacturing components is an important step to evaluate patient safety.... read more »
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» Featured Video
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  On-Demand Webinar: Development and Validation of a Platform Assay Method Using Variable Pathlength Technology for Oligonucleotide Drug Products
This webinar will share Ionis’ experience with developing and validating a platform SoloVPE® in-process assay method for GMP manufacturing of ... watch »
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  On-Demand Webinar: Unified Particle Analysis by Raman and Infrared Microscopy
In this webinar you’ll learn: Identification of unknown particles in a wide variety of manufacturing processes. Reverse engineering and failure ... watch »

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» Featured Products
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  BARETab TM PH
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» Featured Whitepaper
eBook: Primary Packaging for Optimized Fill & Finish
Without effective, well-thought-out primary packaging, the drugs made by the global pharmaceutical industry would not be as effective as they are. Defects on the glass surface are a major cause of ... read more »

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| Events
EVENT
  9th Annual Immuno-Oncology Summit
Westin Copley Place, Boston, MA & Online –  10/04/2021
Over the past 9 years, CHI's Immuno-Oncology Summit has become the leading annual meeting focusing on the latest applied research, providing ...
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EVENT
  Ophthalmic Drugs Conference
London, UK –  11/22/2021
The global ophthalmic drug market is forecast to surpass $60 billion USD by 2025 with increasing focus from the industry on alternative delivery ...
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