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

772. Enforcement policy for non-invasive remote monitoring devices used to support patient monitoring during the coronavirus disease 2019 (COVID-19) public health emergency (revised): guidance for industry and Food and Drug Administration staff

773. Temporary policy for preparation of certain alcohol-based hand sanitizer products during the public health emergency (COVID-19)

774. Policy for temporary compounding of certain alcohol-based hand sanitizer products during the public health emergency: immediately in effect guidance for industry

776. Cytomegalovirus in transplantation: developing drugs to treat or prevent disease

778. 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

779. Supplements for Approved Premarket Approval (PMA) or Humanitarian Device Exemption (HDE) Submissions During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency: guidance for industry and Food and Drug Administration staff

780. Postmarketing adverse event reporting for medical products and dietary supplements during a pandemic