PPT-ClinicalTrials.gov – How to Register Your Trial

1 ClinicalTrialsgov Operated by the National Library of Medicine NLM Each institution has an institutional account Individual investigatorsemployees are given user profiles on that account. June 26, 2014. .. ClinicalTrials.gov and FDAAA for NIH Grantees. David Curren. Special Assistant to the Office Director. Officer of Policy for Extramural Research Administration . Objectives for This Section. February 24, 2015. c. linicaltrials.gov. Notice of Proposed Rule Making (NPRM). November 19, 2014 - HHS published a NPRM for Clinical Trials Registration and Results Submission to clarify existing requirements for registering and submitting results and to implement the statutory requirement for expansion of the registry and results data bank.. NLM Update. May 22, 2012. Seattle, WA. Sheldon Kotzin. kotzin@nlm.nih.gov. 1968 Associate. Group Photo. Kochi, . Alpi. , Murphy, . Crummett. , Walton. What NLM Systems Provide. Dependence on NLM Systems. What Do I Need to Know? . Presenter Name and contact Info. Be aware that…. Any PowerPoint presentation can only be an introduction to a topic. . This subject is complex – this will point you to many other resources – and our office is happy to assist you further. . 1. ClinicalTrials.gov. Operated by the National Library of Medicine (NLM). UC Davis. has an institutional account. Individual investigators/research staff are given user access on that account. Each study gets only one record, regardless of number of sites. National network of libraries of medicine. Middle . atlantic. region. But first: housekeeping. ClinicalTrials.gov: New HHS and NIH Trial Reporting Requirements. with Becky Williams from NIH . (recorded May . 1. ClinicalTrials.gov. Operated by the National Library of Medicine (NLM). UC Davis. has an institutional account. Individual investigators/research staff are given user access on that account. Each study gets only one record, regardless of number of sites. Everything You Ever Wanted to Know About ClinicalTrials.gov (Slides for presentation only.) Deborah A. Zarin, M.D. Director, ClinicalTrials.gov May 2010 1 Background 2 What’s All The Fuss About? Suppression of research results impedes the scientific process Mohammad . Sadrosadati. Amirhossein. . Mirhosseini. Seyed. . Borna. . Ehsani. Hamid . Sarbazi. -Azad. Mario . Drumond. Babak. . Falsafi. Rachata. . Ausavarungnirun. Onur. . Mutlu. Register file size limits GPU scalability . ClinicalTrials.gov NCT02328898. A Permanent Polymer . Zotarolimus. -eluting Stent versus a Polymer-Free . Amphilimus. -eluting Stent in all-comers;. Results of the ReCre8 Trial. R Rozemeijer, M Stein, M Voskuil, R van . University of Maryland School of Nursing. Noon Lecture. February 12, 2019. Presented by: Anthony Keyes, MBA, PMP. . . Director. Aliya Lalji, MD. Clinical Research Compliance Specialist. of Medical Librarians. Network of the National Library of Medicine. Southeastern Atlantic Region. Liz Waltman / . ewaltman@hshsl.umaryland.edu. . Network of the National Library of Medicine. Trainings. FORMAT OF A TRIAL BALANCE . Trial Balance as on (DATE). ITEMS RELATED WITH THE PREPARATION OF TRIAL BALANCE. Public Pressure to Enforce Final Rule. TranspariMED. /UAEM. Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study. Devito. NJ, Bacon S, . Goldacre.