Insights On CONTRACT PHARMA MANUFACTURING
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Extractables And Leachables Testing
4/9/2024
Learn how to navigate the extractables and leachables regulatory landscape and implement best practices for leachables analysis in your pharmaceutical development process.
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Pharmaceutical Solid-State Studies
4/9/2024
Solid-state characterization meticulously analyzes the physical properties of a drug in its solid form. Understand how this analysis is integrated throughout the drug development lifecycle.
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Host Cell Impurities, Bioassays, Micro-Flow Imaging
4/9/2024
Ensuring the safety and efficacy of cutting-edge biopharmaceuticals hinges on meticulous quality control measures. Explore the role of qPCR and MFI in safeguarding drugs from potential contamination.
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Leveraging Inductively Coupled Plasma Mass Spectrometry
4/9/2024
Explore how utilizing ICP-MS can help pharmaceutical companies ensure the safety and effectiveness of their products, ultimately benefiting both patients and the industry as a whole.
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Reducing ADC Timelines With Integrated Development And Manufacturing Services
4/8/2024
ADCs have proven to be highly effective in cancer treatment, but their manufacturing poses challenges. Learn how a CDMO partner can help bring these treatments to patients safely and efficiently.
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Downstream Strategies To Accelerate Preclinical Development Timelines
4/3/2024
As recombinant protein-based products accelerate toward IND, reliable process development methods are critical to meet demand. Review case studies to learn how expedited timelines can be achieved.
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Reducing Costs Via Automated And Closed Systems
3/27/2024
By embracing these advanced technologies, learn how you can streamline your operations, enhance accuracy, and mitigate risks effectively.
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Gain Support For Your Regulatory Submission Process
3/27/2024
Join us in this video as we delve into invaluable tips, cutting-edge tools, and unwavering support that Cytiva offers to facilitate your documentation progress.
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Cell Therapy Process Development Made Easy
3/27/2024
Explore how Fast Trak™ process development services offered by Cytiva can guide you through achieving GMP compliance in your cell therapy manufacturing process.
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Bridging The Gap: Key Considerations In Biologic Technology Transfer
3/21/2024
Technology transfer is a critical step in ensuring the successful production of high-quality biologics. Explore nine key considerations involved in the technology transfer of monoclonal antibodies.