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Discover how early-stage device planning—featuring task analysis, physical comparisons, and human factors studies—can help pharma partners reduce regulatory risk and strengthen ANDA submissions.
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Explore how a drug device developer’s pre-ANDA strategy consisting of task analysis, physical comparisons, and formative comparative use human factors studies can help support successful ANDA submissions.
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Learn how a drug device developer is helping pharma partners de-risk and navigate their ANDA submission with greater confidence through early-stage comparative analysis and formative human factors studies.
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BD Vystra™ Disposable Pen
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Approved in more than 40 countries around the world, the BD Vystra™ Disposable Pen is a commercially proven solution designed for use with a wide range of fixed and variable dose therapies.
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