European Pharmaceutical Review

💻 Join our upcoming webinars designed to expand your knowledge, sharpen your skills, and keep you at the forefront of your field. Whether you're looking to stay updated or explore new areas, these sessions are the perfect opportunity for professional growth. 📅 The future of contamination control in pharma: from compliance to innovation Explore the benefits of accelerated microbial identification using MALDI-TOF mass spectrometry in pharmaceutical contamination control strategies. 🔗 Register here: https://lnkd.in/eFVGRW9D 📅 The Future of Sterility Testing: One-Day Results with Advanced RT-rt PCR Technology Find out how RT-rt PCR is revolutionising sterility testing and discover a unique approach that provides reliable one-day results and enhanced sensitivity and detection capabilities. 🔗 Register here: https://lnkd.in/ekDZzTMd 📅 The Future of Drug Formulation – 2026 & Beyond  Hear expert forecasts on formulation trends, technology, and innovation.  🔗 Register here: https://bit.ly/44gUWyQ

🔬 New frontiers in AAV analytics! Researchers from Sartorius BIA Separations and BridgeBio Gene Therapy present a streamlined, high‑throughput purification protocol for rAAV lysates – boosting purity, speeding analysis, and reducing development costs. Check out the full article to dive into the method and results >> https://lnkd.in/eaTxg_qr

⏳ There’s just one week to go – have you secured your seat? Our webinar on the future of contamination control in pharma is happening on 22 October – and spots are filling up fast! Join our expert speakers from Nivagen Pharmaceuticals, Inc. – Nilkantha Banerjee, MS, MBA, PGD, Olivia Matsumoto-Elliott, and Adam Peters – as they share insights on how rapid microbial identification is transforming contamination control, helping you prevent audit failures and stay compliant. Don’t miss your chance to: ✔️ Learn how global regulatory bodies define and assess CCS ✔️ Explore how innovations such as automation, data analytics and real-time monitoring are transforming contamination control practices ✔️ Discuss projections for industry evolution, including advancements in rapid testing methods and their implications for QA and operational efficiency. 👉 Register here: https://lnkd.in/gH_7egm6 This webinar is in association with Bruker • Microbiology & Infection Diagnostics.

Access your free copy of this application note In pharmaceutical formulations, your packaging can make - or break - the product. Explore how moisture and odour control are critical to protecting efficacy, shelf life, and patient safety. From smart desiccant strategies to regulatory considerations, this is a must-read for anyone in drug development, formulation, or packaging. Read here >> https://lnkd.in/eTm3yYkG

Join us tomorrow! This is your last chance to register for our live webinar, Mastering Impurity Profiling: USP’s Evolving Standards and Strategies. Join us and ask your questions live to our expert, Christian Zeine, during the Q&A session. This is your opportunity to get direct answers on US Pharmacopeia's evolving standards. Register now and make sure you don't miss out on this live, interactive event: https://bit.ly/4p6IWs4 #Webinar #Pharma #Impurity #Impurities #QualityControl #Q&A

The European Pharmaceutical Review will be at CPHI Frankfurt in October. Editor Dominic Tyer and Ryan Clarke will be there to soak up the industry knowledge, share insights, and network! If you'd like to talk, please reach out!

BENEO's newest study shows that galenIQ™ is an excellent choice as a binder in both twin screw granulation and high-shear granulation processes, combining reliable granule formation with rapid tablet disintegration and a sugar-like taste for improved patients' compliance. ✨ Interested in finding out how galenIQ™ can seamlessly fit into your continuous manufacturing? Visit BENEO at CPHI 28-30 October at booth #80L70 to talk to the team!

💻 New webinar alert: Automating quality control testing for radiopharmaceutical production This webinar showcases a rapid microbial method that can help to address the time to result challenge posed by short shelf-life radiopharmaceuticals. Key learning points include: 🔹 Understand the benefits of full workflow microbiology quality control testing automation in radiopharmaceutical production 🔹Learn about ITM’s implementation journey and considerations when evaluating the technology 🔹Find out how the advanced optics and microcolony detection capabilities of Growth Direct® technology impact time to result (TTR). Secure your spot today >> https://bit.ly/3IYn95l This webinar is in association with Rapid Micro Biosystems

What can you expect to learn from Christian Zeine on 15th October at 1:00PM? He'll be sharing key insights on: ✅ How US Pharmacopeia addresses impurities in general ✅ How Pharmaceutical Analytical Impurities can complement your work ✅ Specific approaches to major challenges like Nitrosamines His experience working with scientific experts and stakeholders makes his perspective invaluable. Don't miss out! 👉 Register now: https://bit.ly/4p6IWs4 #Webinar #Pharma #Impurity #USP #Pharmaceuticals #Impurities #QualityControl #Q&A