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: To provide Congress with transparent data on the FDA's progress in managing the "backlog" of postmarketing studies that drug companies are required or have committed to conduct after a drug is approved.

: These reports typically track the number of open PMRs/PMCs, the percentage that are on schedule versus delayed, and the FDA's efficiency in reviewing the final study reports submitted by manufacturers. (571 KB)

: The North Carolina Department of Health and Human Services (NC DHHS) provides a Post-Overdose Response Teams (PORT) Overview (571 KB) that details community-based strategies for responding to opioid overdoses. : To provide Congress with transparent data on