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321. Considerations for defining rural places in health policies and programs

322. Considerations for design, development, and analytical validation of next generation sequencing (NGS)--based in vitro diagnostics (IVDs) intended to aid in the diagnosis of suspected germline diseases: guidance for stakeholders and Food and Drug Administration staff

324. Considerations for the development of dried plasma products intended for transfusion

325. Considerations for the inclusion of adolescent patients in adult oncology clinical trials

326. Considerations for the use of real-world data and real-world evidence to support regulatory decision-making for drug and biological products: guidance for industry

327. Considerations in demonstrating interchangeability with a reference product

328. The consistently low percentage of Medicare enrollees receiving medication to treat their opioid use disorder remains a concern

330. Consumer antiseptic wash final rule: questions and answers : (Small Entity Compliance Guide)