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33. Good manufacturing practice considerations for responding to COVID-19 infection in employees in drug and biological products manufacturing

36. COVID-19 public health emergency: general considerations for pre-IND meeting requests for COVID-19 related drugs and biological products : guidance for industry and investigators

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

40. Review timelines for applicant responses to complete response letters when a facility assessment is needed during the COVID-19 public health emergency