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6201. Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process": guidance for industry and Food and Drug Administration staff

6206. 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

6207. Wholesale distributor verification requirement for saleable returned drug product and dispenser verification requirements when investigating a suspect or illegitimate product: compliance policies : guidance for industry

6209. Survey of emergency department practices in Pennsylvania hospitals to protect patients and staff

6210. Strategies to improve outcomes in nursing home residents with modifiable risk factors for respiratory tract infections