HOW A TEAM OF ON-SITE VALIDATION EXPERTS OFFSET THE CHALLENGES OF GETTING A NEW BIOPHARMACEUTICAL MANUFACTURING FACILITY UP AND RUNNING
Managing a new facility start-up can seem like a constant race against the clock.
In 2016, with limited in-house resources to dedicate to the validation of a new facility, a top-20 U.S. biopharmaceuticals manufacturer faced the challenge of building a new active pharmaceutical ingredient manufacturing facility from the ground up.
Learn how engaging Azzur Group for full-scale GMP-compliance project management and execution allowed the client to meet their goal.
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