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1. Medical product communications that are consistent with the FDA-required labeling: questions and answers

2. Drug and device manufacturer communications with payors, formulary committees, and similar entities: questions and answers : guidance for industry and review staff

3. Developing and responding to deficiencies in accordance with the least burdensome provisions: guidance for industry and Food and Drug Administration staff

4. Best practices for communication between IND sponsors and FDA during drug development: guidance for industry and review staff : good review practice