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  1. ... page. Print What are the requirements for updating clinical trial registration information when a Human Subjects Review Board approves a ... in the clinical trial, updates to any relevant clinical trial registration information data elements must be submitted not later than ...
  2. ... page. Print When must I submit the required clinical trial registration information? Views: The regulations at 42 CFR 11.24( ... of a device product and is not a clinical trial, the registration information specified in section 402(j)(2)(A)(ii) ...
  3. ... version of the page. Print When is required clinical trial results information due? Views: For applicable clinical trials that are subject to 42 CFR 11. ...
  4. ... Modernization Priorities, by Strategic Goal ............................................... ................................................ ...................................14 Goal 1: Clinical Trial Information Is Current, Complete, and Reliable 14 Goal 2: ... NIH Policy on the Dissemination of NIH-Funded Clinical Trial Information, NPRM = Notice of Proposed Rulemaking, WHO = World Health ...
  5. ... on the Modernization Strategic Goals ............................................... .........................14 Goal 1: Clinical Trial Information Is Current, Complete, and Reliable 14 Goal 2: ... NIH Policy on the Dissemination of NIH-Funded Clinical Trial Information, NPRM = Notice of Proposed Rulemaking, WHO = World Health ...
  6. ... on the Modernization Strategic Goals ............................................... .........................12 Goal 1: Clinical Trial Information Is Current, Complete, and Reliable 12 Goal 2: ... outcomes, or effects, of the modernization effort: (1) Clinical trial information is current, complete, and reliable; (2) Anyone can ...
  7. ... the Protocol Registration and Results System (PRS). The clinical trial information provided by this stakeholder group is listed on ... through ClinicalTrials.gov. 3. Data researchers , who use clinical trial information to study the clinical research enterprise, such as ...
  8. ... all the different aspects they face either using clinical trial information or needing to provide clinical trial information, and then all the years moving forward would ...
  9. ... the project manager for the multi-agency AIDS Clinical Trials Information Service (ACTIS) and the HIV/AIDS Treatment Information ... will continue to provide access to AIDS-related clinical trials information (through ClinicalTrials.gov) and federally approved treatment guidelines. ...
  10. ... the project manager for the multi- agency AIDS Clinical Trials Information Service (ACTIS) and the HIV/AIDS Treatment Information ... AIDSinfo.” This service provides access to AIDS-related clinical trials information (through Clinicaltrials.gov) and federally approved treatment guidelines. ...
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