Transparency on trial: How to navigate FDAAA 801 final rule implementation and compliance
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A service of the U.S. National Institutes of Health Module 1: Clinical Trials and Requirements for Registration and Results Reporting. - ppt download
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Transparency on trial: How to navigate FDAAA 801 final rule implementation and compliance
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Clinical Trial Results Transparency and the Changing Paradigm of Medi…
Progress and Deficiencies in the Registration of Clinical Trials | NEJM
Clinical Trials gov Results Reporting Unique Evidence and
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ClinicalTrials.gov Results Reporting, Unique Evidence, and the Role of Medical Librarians SCR CONNECTions March 19, ppt download
First Action for Non-Compliance with FDAAA section 801 Requirements
Requirements for Registering & Reporting NIH-funded Clinical Trials in ClinicalTrials.gov | grants.nih.gov
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PPT - Everything You Ever Wanted to Know About ClinicalTrials PowerPoint Presentation - ID:285237
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Publication and reporting of clinical trial results: cross sectional analysis across academic medical centers | The BMJ
FOCUS ON NLM RESOURCES: CLINICALTRIALS.GOV. WHAT IS A CLINICAL STUDY? Research study using human subjects. Volunteers may have a certain disease or. - ppt download
ClinicalTrials.gov Requirements | Human Subjects Office
FAQS and facts about clinical trials and ethical errors - Journal of Plastic, Reconstructive & Aesthetic Surgery
