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As plans are working with their actuaries and 2025 bids, the financial impacts of the expected increased GLP-1 utilization must be considered in addition to the Part D Redesign plan liability

Key quality indicators include: the pharmacy conducts in-house stability testing on their specific formulations, they perform sterility testing on each batch, they follow USP 797 guidelines for sterile compounding, and they can provide certificates of analysis upon request

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