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    • Network adequacy for behavioral health: existing standards and considerations for designing1
    • Nevada Medicaid Fraud Control Unit: 2018 onsite inspection1
    • New Hampshire Medicaid Fraud Control Unit: 2017 onsite review1
    • New Jersey Medicaid Fraud Control Unit: 2017 onsite review1
    • New Jersey could better ensure that nursing homes comply with federal requirements for life safety, emergency preparedness, and infection control1
    • New Mexico Medicaid Fraud Control Unit: 2020 review1
    • New York Medicaid Fraud Control Unit: 2017 onsite inspection1
    • New York did not ensure that a managed care organization complied with requirements for denying prior authorization requests1
    • Newborn health: federal action needed to address neonatal abstinence syndrome : report to Congressional addressees1
    • Next steps: improving the Medicaid buy-in for workers with disabilities1
    • No free lunch?: current challenges facing National School Lunch and School Breakfast Programs1
    • Non-clinical and clinical investigation of devices used for the treatment of benign prostatic hyperplasia (BPH): guidance for industry and Food and Drug Administration staff1
    • Non-clinical performance assessment of tissue containment systems used during power morcellation procedures: guidance for industry and Food and Drug Administration staff1
    • Nonallergic rhinitis: developing drug products for treatment1
    • Nonclinical considerations for mitigating nonhuman primate supply constraints arising from the COVID-19 pandemic1
    • Nonclinical evaluation of the immunotoxic potential of pharmaceuticals: guidance for industry1
    • Nonclinical testing of orally inhaled nicotine-containing drug products1
    • Nonmetastatic castration-resistant prostate cancer: considerations for metastasis-free survival endpoint in clinical trials1
    • Nontuberculous mycobacterial pulmonary disease caused by mycobacterium avium complex: developing drugs for treatment : guidance for industry1
    • Notifying CDRH of a permanent discontinuance or interruption in manufacturing of a device under Section 506J of the FD&C Act during the COVID-19 public health emergency (revised): guidance for industry and Food and Drug Administration staff1
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