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31 results
  1. ... Pilot Projects Product Surveillance, Postmarketing Adverse Drug Reaction Reporting Systems Clinical Trials, Phase IV as Topic Pharmacovigilance Program Evaluation Reproducibility of Results Dimensional Measurement Accuracy Validation ...
  2. ... Research Performance Progress Report (RPPR) Submission Validations for Clinical Trial ... for the Human BioMolecular Atlas Program (U54 Clinical Trial Not Allowed). (RFA-RM-21- ...
  3. ... the ClinicalTrials.gov program and praised it. The program continued to provide ... and for reporting to results databases. For example, a key activity ...
  4. ... Postmarketing E05.337.800.120...........................................Adverse Drug Reaction Reporting ... of Results E05. ...
  5. ... Department of Agriculture (USDA); enhancing registration and results ... extramural programs. NLM will continue to leverage the National Network ...
  6. ... Department of Agriculture (USDA); enhancing registration and results ... extramural programs. NLM will continue to leverage the National Network ...
  7. ... Postmarketing E05.337.800.120 Adverse Drug Reaction Reporting Systems E05.337.800.200 Clinical Trials, Phase IV as Topic E05.337.800.600 Pharmacovigilance E05.337.800.800 Prescription Drug Monitoring Programs E05.337.820 Program Evaluation E05.337.851 ...
  8. ... to perform economic analyses as part of its clinical trials. The Food and ... Event Reporting System on adverse events and medication error reports ...
  9. ... clinical trials. Unfortunately, the contents of published papers reporting on clinical trials are often heterogeneous with respect to the types ...
  10. ... the system, and promoting standards of transparency in clinical research through trial registration and results reporting. This information was communicated to a broad range ...
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