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| Webinar: Navigating Regulatory Shifts: EU GMP Annex 1 and USP 382 | Join our webinar to explore how to build a robust, evolving Contamination Control Strategy (CCS) aligned with EU GMP Annex 1 and upcoming USP <382> standards. Experts from West—Dr. Ana Kuschel, Todd Jasinski, and Daria Miller—will share insights on supplier alignment, risk mitigation, and fostering a quality-driven culture to help manufacturers meet regulatory expectations and enhance patient safety. Click here to learn more. |
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| Opportunities In Preclinical Development | White Paper | IDBS UK HQ | Every domain produces critical data and this data and contexual information should be captured and managed in the most effective and robust manner. |
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| Unpacking FDA's Final Rule To Regulate LDTs | White Paper | Ideagen | Examine how the FDA's rule redefines diagnostic testing by classifying laboratory-developed tests (LDTs) as medical devices to ensure stricter oversight and consistent standards for safety and efficacy. |
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| Considerations To Purchasing Low-Cost Manufacturing Equipment | Application Note | By Mike Coyne, Federal Equipment Company | No one can deny the cannabis industry is one to watch. Learn how used process and packaging equipment for the marijuana and CBD industry can fill a growing need for manufacturing equipment. |
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| Thermal Analysis In The Pharmaceutical Industry | Application Note | By Monika Schennen, TA Instruments | Thermal analysis techniques provide valuable insights into pharmaceutical material properties to ensure compatibility, stability, and quality control in drug development and production processes. |
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| Efficient Blending Of Viscous Solutions In Bioprocessing | Application Note | By David Menahem and Stéphane Giaconia, Sartorius | Efficiency in bioprocessing and achieving rapid mixing across various viscosities is crucial for consistent biopharmaceutical product quality. Uncover more about the benefits of this mixer. |
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| How To Secure A Sustainable Supply Of API | Article | Pfizer CentreOne | How can pharma companies secure the supply of vital APIs and intermediates and maintain consistent manufacturing costs? These steps minimize supply chain insecurity in a rapidly changing market. |
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| Improving Medical Device Sustainability | Article | By Molly Wagle, dsm-firmenich | Product design, production methods, and supply chain can be leveraged to positively impact sustainability through effective planning. |
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By Sabyasachi Ghosh, Future Market Insights | The small molecule contract development and manufacturing (CDMO) sector continues to expand in 2025. As the small molecule CDMO landscape expands, it is still fragmented, driving both M&A and big capital projects to get ahead. | |
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