Healthcare

PRODUCTS

  • Biomanufacturers need a flexible and scalable approach to fluid handling to overcome complex regulatory demands and improve production efficiency. Fluid handling solutions from Avantor®, including agile single-use solutions and Masterflex® peristaltic pumps, enable biomanufacturers to bring breakthrough therapies to market quickly and safely.

    Masterflex® peristaltic pump systems, engineered for a long life, provide superior accuracy and repeatability, ensuring optimal performance from the research phase to scaled-up production.

  • Honeywell Manufacturing Excellence makes it easier than ever for life sciences manufacturers of all sizes and complexities to achieve outstanding outcomes.

  • What is included in Forge's DMF?

    DMFs come in all shapes and sizes, but Forge's DMF includes the following components:

    • Information on our critical raw materials, including our Ignition Cells™ and pEMBR™ adenovirus helper plasmid
    • An overview of our platform AAV manufacturing process
    • Process controls
    • Facility layout and engineering information
    • And more!
  • Take Control of Product Quality by Error-Proofing Production Operations

    Nothing is more important than product quality. As it becomes more complex to manage quality and stay current on compliance in today’s world, efforts to reduce cost and increase transparency make it challenging to sustain high quality levels.

    When manual processes and homegrown systems fall short, Plex Quality Management System (QMS) can help you take the guesswork out of quality management and error-proof your production operation. Plex QMS offers manufacturers increased quality visibility and real-time data capture to ensure repeatability, predictability, and compliance management.

    Plex QMS makes it possible to digitally manage quality with accurate, real-time quality content aligned to industry and product requirements. And you gain increased operational excellence.

  • Robust quality and regulatory support protects our clients and ultimately patients.

    Focus on compliance and continuous improvement

    At the Center for Breakthrough Medicines, our quality management systems and regulatory services provide the highest level of compliance, control, and oversight for our client programs from the inception of the clinical trial through commercialization. Having a dedicated regulatory team on site supporting your program will allow for real-time process information and analytical data to be procured, evaluated, and applied to your submission filing. The requirements of an IND/BLA are complicated and can be difficult to interpret. By partnering with CBM, we can utilize our strong relationships with the health authorities and collaborate with you to make sure your filing meets the stringent requirements set forth by the agencies, minimizing any potential delays to your program resulting from the review process.

WHITE PAPERS AND CASE STUDIES

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