Tuesday, May 28, 2019 5:40:02 PM
o More frequent meetings with FDA to discuss the drug's development plan and ensure collection of appropriate data needed to support drug approval
o More frequent written communication from FDA about such things as the design of the proposed clinical trials and use of biomarkers
o Eligibility for Accelerated Approval and Priority Review, if relevant criteria are met
o Rolling Review, which means that a drug company can submit completed sections of its Biologic License Application (BLA) or New Drug Application (NDA) for review by FDA, rather than waiting until every section of the NDA is completed before the entire application can be reviewed. BLA or NDA review usually does not begin until the drug company has submitted the entire application to the FDA
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