Covid-19 manufacturing roundup: Emergent starts clean-up effort after disastrous Form 483; Eli Lilly expands licenses for Indian partners
After botching millions of doses of a Covid-19 vaccine, being overtaken by the FDA and shaking up its leadership team, Emergent has completed a comprehensive quality enhancement plan, the company announced Wednesday. The move comes after the FDA issued the firm a disastrous Form 483 that noted numerous quality control and training issues.
“We have already started making improvements and we are fully committed to making the necessary short — and long — term enhancements to meet or exceed FDA standards,” the statement said.
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