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Compliance with legal requirement to report clinical trial results on  ClinicalTrials.gov: a cohort study - The Lancet
Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study - The Lancet

ClinicalTrials.gov FAQs
ClinicalTrials.gov FAQs

Home - ClinicalTrials.gov
Home - ClinicalTrials.gov

A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials  Register (EudraCT)
A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials Register (EudraCT)

Upload Human Subjects Data Directly to ClinicalTrials.gov
Upload Human Subjects Data Directly to ClinicalTrials.gov

ClinicalTrials.gov Tip of the Week: Seife et al. v. HHS et al.: Results  Must be Submitted for “pACTs” to Clinical Trials.gov
ClinicalTrials.gov Tip of the Week: Seife et al. v. HHS et al.: Results Must be Submitted for “pACTs” to Clinical Trials.gov

Clinical Trials gov Protocol Registration System PRS Registration
Clinical Trials gov Protocol Registration System PRS Registration

Support for ClinicalTrials.gov Compliance | CCTS
Support for ClinicalTrials.gov Compliance | CCTS

ClinicalTrials.gov Hot Off the PRS! Update -- Aug. 6, 2019
ClinicalTrials.gov Hot Off the PRS! Update -- Aug. 6, 2019

CTSI | ClinicalTrials.gov PRS Training
CTSI | ClinicalTrials.gov PRS Training

ClinicalTrials.gov FAQs
ClinicalTrials.gov FAQs

ClinicalTrials.gov Modernization Effort: Beta Releases Now Available | LJ  INFOdocket
ClinicalTrials.gov Modernization Effort: Beta Releases Now Available | LJ INFOdocket

ClinicalTrials.gov FAQs
ClinicalTrials.gov FAQs

ClinicalTrials.gov
ClinicalTrials.gov

ClinicalTrials.gov Page
ClinicalTrials.gov Page

FDA's First Notice of Noncompliance with ClinicalTrials.gov requirements
FDA's First Notice of Noncompliance with ClinicalTrials.gov requirements

ClinicalTrials.gov Info
ClinicalTrials.gov Info

Support for ClinicalTrials.gov Compliance | CCTS
Support for ClinicalTrials.gov Compliance | CCTS

ClinicalTrials.GOV
ClinicalTrials.GOV

ClinicalTrials.gov updates the PRS Guided Tutorials, step-by-step  instructions for data providers - NCBI Insights
ClinicalTrials.gov updates the PRS Guided Tutorials, step-by-step instructions for data providers - NCBI Insights

Prs Login Page - ClinicalTrials.gov PRS: Login
Prs Login Page - ClinicalTrials.gov PRS: Login

Upload Human Subjects Data Directly to ClinicalTrials.gov
Upload Human Subjects Data Directly to ClinicalTrials.gov

A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials  Register (EudraCT)
A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials Register (EudraCT)

Medical Writing | Public Disclosure | Clinical trial results disclosure on  ClinicalTrials.gov and EudraCT
Medical Writing | Public Disclosure | Clinical trial results disclosure on ClinicalTrials.gov and EudraCT

ClinicalTrials.gov and CTRP - DF/HCC
ClinicalTrials.gov and CTRP - DF/HCC

ClinicalTrials.gov | Office of the Vice President for Research
ClinicalTrials.gov | Office of the Vice President for Research

ClinicalTrials.gov Requirements - Center for Clinical and Translational  Science | UAB
ClinicalTrials.gov Requirements - Center for Clinical and Translational Science | UAB

ClinicalTrials.gov trial registration submission cycle. JHUSOM: Johns... |  Download Scientific Diagram
ClinicalTrials.gov trial registration submission cycle. JHUSOM: Johns... | Download Scientific Diagram