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There are two primary filling methods for pre-filled syringes. Explore the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.
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The revised Annex 1 regulation has prompted the pharmaceutical industry to strategize on the best compliance method, focusing on progress towards harmonizing regulations across the pharmaceutical manufacturing industry. It emphasizes the vital roles of automated and barrier technology in ensuring medicinal production safety and quality.
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Establishing early and clear tech transfer strategies is a key component of a holistic approach to drug development. When key technologies can seamlessly transfer from system to system, it reduces the need for revalidation and saves valuable time. Learn about the role that capable fill/finish solutions play in this process.
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The pharmaceutical manufacturing industry is seeing growth in high-value liquid pharmaceuticals. Learn about flexible aseptic processing system that provides modular, semi-automated, and fully automated solutions to meet demands at all stages of development. The system can process a variety of vials, syringes, and cartridges on the same line.
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When it comes to fill-finish manufacturing of parenteral liquid pharmaceuticals, your choice of barrier technology is crucial. Assess air handling obstacles and learn how a fully integrated, turnkey barrier and fill-finish technology can help pave your way to achieving high levels of product integrity and viability.
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