PharmTech Group
@PharmTechGroup
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Bringing you the latest news, trends, and insight circulating the global pharmaceutical development and manufacturing industry.
UK + USA
Joined February 2009
ArisGlobal brought together experts to discuss the industry's implementation of ISO's #IDMP standards and how data are still not being optimized as it should be. #drugidentification #serialization. https://t.co/ypuxLDMRpb
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Europe is overhauling pharma regulations to boost access, affordability, and innovation, targeting market exclusivity and antimicrobial resistance. Stay informed: https://t.co/CAPcKPtYnn
#EMA #AMR
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Discover how automation is transforming pharmaceutical manufacturing. Cynthia Challener explores how cost and complexity are accelerating adoption of advanced processes. Read more: https://t.co/znB1P2ftvx
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Unlock expert insights on effective batch recovery! Susan J. Schniepp shares best practices for pharmaceutical manufacturing in the latest #AsktheExpert from PharmTech. Read more:
pharmtech.com
Susan J. Schniepp, distinguished fellow at Regulatory Compliance Associates, a Nelson Labs Company, outlines the importance of batch recovery procedures in pharmaceutical manufacturing.
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Cheryl Barton takes a look at European biotechs that are developing innovative high-throughput screening methods to improve in vitro–in vivo translation and accelerate drug discovery. #highthrougputscreening #drugdevelopment
https://t.co/E2Q8020jyO
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This session covers best practices for sourcing and managing comparator products to help sponsors and clinical supply teams navigate selection, procurement, and distribution—guided by insights from Catalent’s global experience. Register Now: https://t.co/nTUx0d5pKz
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Everything from the week that was on PharmTech! Full video recap here: https://t.co/2OTI72VbWv
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A report from @UKParliament forebodes a warning to the #pharma industry about the importance of being able to commercialize R&D. Read about it here: https://t.co/4Zk3NiuewY
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Catch up on everything we've covered this week, including exclusive interviews from #AAPS PharmSci 360, in our weekly roundup:
pharmtech.com
Accelerated drug development insights using AI/digital twins, advanced bioanalysis, targeted delivery, and optimized formulation stability models.
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Drug Digest: Closing the Gap in Modern Process Control and Automation for Quality Biopharma quality control is being revolutionized by advanced analytics and digital transformation through a synergy that boosts quality and scalability. Register Now: https://t.co/o5H2K4bxga
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A partnership between @ChiesiGroup and an @abbvie subsidiary aims to tackle lysosomal storage disorders. Story here: https://t.co/DSRszJOOOT
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Standardizing Endonuclease Activity: What You Need to Know About USP As regulatory expectations rise, standardized, activity-based methods are key. See how Eurofins validated USP’s proposed method for fitness-for-purpose. Register for the webinar: https://t.co/Kb6mxKAZH5
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Join this expert-led webinar to learn how advances in automation, artificial intelligence (AI), and predictive analytics are transforming the way companies plan, produce, and deliver life-saving products. Register Now: https://t.co/mbk1HaNsgX
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Long Yuan, PhD, director of the Department of Drug Metabolism and Pharmacokinetics at @biogen explains how artificial intelligence, machine learning, and large language models are used in performing bioanalysis. #AAPSPharmSci360
https://t.co/owSfJ7sw6D
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Dr. Mark Arnold, owner and principal, Bioanalytical Solution Integration, explains how bioanalysis enhances bio/pharmaceutical drug development. #AAPSPharmSci360
https://t.co/ZAg5aWFj2n
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Watch Steve Lowes, senior director of Scientific Affairs at IQVIA Laboratories, explain how method validation is performed for biomarker bioanalysis. #AAPSPharmSci360
https://t.co/RqKxqdAiup
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Drug Digest: Closing the Gap in Modern Process Control and Automation for Quality Biopharma quality control is being revolutionized by advanced analytics and digital transformation through a synergy that boosts quality and scalability. Register Now: https://t.co/3w9WmWU3pc
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Join this expert-led webinar to learn how advances in automation, artificial intelligence (AI), and predictive analytics are transforming the way companies plan, produce, and deliver life-saving products. Register Now: https://t.co/9X0feReaW2
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Accelerating Quality: How to Partner Successfully for Rapid, Compliant Microbiological Testing Join Eurofins to explore how to build successful partnerships, choose the right lab, and meet current regulatory expectations:
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Discover how Datwyler’s solutions are engineered to enhance drug stability, ensure functionality and device compatibility, and secure your supply chain from development through delivery. Register Now: https://t.co/6idmHMU7vA
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