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    Why QuVa

    When looking for a partner to be a reliable  extension of your pharmacy operation, it’s critical to select one that is accountable to you and raises the bar for quality and FDA compliance. Learn why and how QuVa is built to lead the future of 503B sterile compounding.

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Day: September 26, 2019

QuVa Pharma Announces Immediate Significant Capacity Increase for Compounded Sterile Injectable Preparations

— Company more than doubles capacity at its New Jersey location through additional production, post compounding and distribution capabilities — SUGAR LAND, TX – September 26, 2019 – QuVa Pharma, Inc. today announced it is completing the next phase of capacity expansion at its Bloomsbury, New Jersey, state-of-the-art cGMP compliant 503B FDA registered manufacturing facility. […]

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