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Home - ClinicalTrials.gov
Home - ClinicalTrials.gov

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

Clinical Trials gov Results Reporting from the Ground
Clinical Trials gov Results Reporting from the Ground

ClinicalTrials.gov FAQs
ClinicalTrials.gov FAQs

ClinicalTrials.gov Registration & Reporting Requirements - ppt download
ClinicalTrials.gov Registration & Reporting Requirements - ppt download

PDF) ClinicalTrials.gov Brief Title: Cholecalciferol to Improve the  Outcomes of COVID-19 Patients ( CARED ) Official Title: Randomized  Controlled Trial of High Dose of Vitamin D as Compared With Placebo to  Prevent
PDF) ClinicalTrials.gov Brief Title: Cholecalciferol to Improve the Outcomes of COVID-19 Patients ( CARED ) Official Title: Randomized Controlled Trial of High Dose of Vitamin D as Compared With Placebo to Prevent

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

ClinicalTrials.gov PRS – How to Register and Maintain a Record - ppt  download
ClinicalTrials.gov PRS – How to Register and Maintain a Record - ppt download

HEALWA
HEALWA

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)

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

Clinical Trials gov How to Register Your Trial
Clinical Trials gov How to Register Your Trial

ClinicalTrials.gov: How to Register Your Trial - Clinical and Translational  Science Institute - University at Buffalo
ClinicalTrials.gov: How to Register Your Trial - Clinical and Translational Science Institute - University at Buffalo

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

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

PDF) 3381 Reducing Problem Records in the Johns Hopkins University  ClinicalTrials.gov Protocol Registration and Results System (PRS)
PDF) 3381 Reducing Problem Records in the Johns Hopkins University ClinicalTrials.gov Protocol Registration and Results System (PRS)

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

PLOS ONE: Primed to comply: Individual participant data sharing statements  on ClinicalTrials.gov
PLOS ONE: Primed to comply: Individual participant data sharing statements on 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)

Clinical Trials gov Results Reporting from the Ground
Clinical Trials gov Results Reporting from the Ground

ClinicalTrials.gov Info
ClinicalTrials.gov Info

ClinicalTrials.gov Page
ClinicalTrials.gov Page

Obstacles to the reuse of study metadata in ClinicalTrials.gov | Scientific  Data
Obstacles to the reuse of study metadata in ClinicalTrials.gov | Scientific Data

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

New Style and New Content for ClinicalTrials.gov. NLM Technical Bulletin.  2012 Jul–Aug
New Style and New Content for ClinicalTrials.gov. NLM Technical Bulletin. 2012 Jul–Aug

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