Jessica Buday

Process validation is a critical step in the successful commercialization of a new biopharmaceutical. In this Q and A, Claudia Berdugo Ph.D., of Catalent Biologics, talks about key strategies and challenges for process validation. Download now. https://ow.ly/waYf50SQ8Us

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Process validation is a critical step in the successful commercialization of a new biopharmaceutical. In this Q and A, Claudia Berdugo-Davis, Ph.D., of Catalent Biologics, talks about key strategies and challenges for process validation. Download now. https://ow.ly/waYf50SQ8Us

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Process validation is a critical step in the successful commercialization of a new biopharmaceutical. In this Q and A, Claudia Berdugo-Davis, Ph.D., of Catalent Biologics, talks about key strategies and challenges for process validation. Download now. https://ow.ly/waYf50SQ8Us

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🗞 Breaking news 🤩 Genezen acquire uniQure's commercial GT manufacturing ops in Lexington!! This strategic acquisition will enable Genezen to deliver late-phase and commercial gene therapy development and manufacturing services to customers around the world. Check out full article below👇 #CDMO #Genezen #GeneTherapy

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PharmTech is expanding our Ask the Expert column to a video series! Experts will answer your questions on quality, manufacturing, formulation, and more in a new video format! If you have a question you would like answered, please send it to [email protected] #PTasktheexpert

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PharmTech is expanding our Ask the Expert column to a video series! Experts will answer your questions on quality, manufacturing, formulation, and more in a new video format! If you have a question you would like answered, please send it to [email protected] #PTasktheexpert

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Discover the P.E.R.F.E.C.T blog series! Dive into our collection of insightful blogs that guide you through selecting the right packaging solution for your injectable drug. Check out the full series! https://lnkd.in/gEg7Ahz6

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Fernand Desjarlais explores how the CDMO industry is currently experiencing a notable wave of leadership changes, including AGC Biologics, Lonza and Catalent Pharma Solutions - reflective of broader shifts within the sector. Read more below: https://lnkd.in/eJ_zVUet #cdmo #leadership #pharmaleaders

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At the AIPIA & AWA Smart Packaging Congress,Anne Marie Mohan reports how Merck and Johnson & Johnson are collaborating on digital display labels, a promising technology poised to enhance clinical supply chain. #pharmaceuticalpackaging #supplychain

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Get ready for Episode 7 of the GxPodcast! 🎙️ This week, we're joined by Chris Lewis, the Vice President of GMP Quality for Umoja Biopharma. Tune in to hear us discuss quality culture and excellence in life sciences. We look at cell and gene manufacturing, the connection between innovation and purpose, and the importance of data management in our industry. Tune in to the full episode here: 🔗 https://lnkd.in/exW4jkBB #GXPodcast #iPharmGxP

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Amgen Announces $1B Manufacturing Expansion In North Carolina Read the news here - https://lnkd.in/gEedEYqS #Amgen #Biotech #PharmaNews #DrugManufacturing #Biomanufacturing #NorthCarolina #HollySprings #BiotechExpansion #SustainableManufacturing

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Stay Ahead with Neopharm Adapting to the BIOSECURE Act? Neopharm provides tailored CRO services and GMP compliance in North America to keep your biopharma operations secure and compliant. Stay ahead with our expert solutions. Learn more: https://hubs.li/Q02Sn3290 Sponsored by Neopharm Labs #Biopharma #Pharmaceuticals #Compliance #BIOSECUREAct #R&D #RegulatoryExcellence #SupplyChainSecurity #Neopharm

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Amgen announced a $1 billion expansion to establish a second drug substance manufacturing facility in North Carolina. The $1 billion facility will incorporate cutting-edge technologies and sustainable practices, aligning with Amgen's commitment to environmental stewardship and manufacturing excellence. In tandem with the existing facility, these investments will create 370 new jobs in the region, supporting a robust biomanufacturing hub. Read more: https://lnkd.in/gyF5xUCv

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Navigating the complexities of developing a biologic? Whatever the phase, presentation, viscosity, or hurdle, rely on Catalent Biologics’ seasoned formulation scientists to help you develop a safe, efficacious and robust drug product. Discover how here: https://ow.ly/QjVo50TKQ8m

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Does your CDMO have an effective contamination control strategy (CCS)? Listen in to hear a few ways that GRAM stays ahead of the curve. https://hubs.la/Q02ChZFm0 #pharma #biotech #contractpharma #fillfinish

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Process validation for cell and gene therapy products is a daunting challenge when scaling up manufacturing. In this snippet from a recent webinar, AGC Biologics' Senior Manager of MSAT reviews the primary considerations for process validation strategy in cell and gene therapy development. Wondering how to overcome these challenges and advance novel therapies from concept to market? View the full webinar to receive expert insights on navigating the journey to FDA/EMA approval: https://hubs.li/Q02Ghx4r0 #CellAndGeneTherapy #GeneTherapy #Biologics #Biopharmaceuticals #FDAApprovalProcess

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Wondering what FDA approvals are on the horizon? Check out this list of 5 key decisions to watch in the fourth quarter of 2024. Stay up-to-date with the latest developments in the industry.

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