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Documents 2011 01 16 NIS Training (Chcuk Generic)

1. NON-INTERVENTIONAL STUDIES? What are they? How do they differ from Clinical Trials?Stuart McCully, PhD 16th January 2011 2. DISCLAIMERAlthough this material contains information…

Documents Building Capacity to Translate Biomedical Research into Practice

NCRR Strategic Plan 2009â2013 Translating Research from Basic Discovery to Improved Patient Care About NCRR Together, NCRRâs four integrated and complementary areas accelerate…

Documents GCP Refresher Training (Chcuk) V2

1. GCP REFRESHER TRAINING A Recap of the Essentials and a Look at What’s NewStuart McCully, PhD29th June 2010 2. DISCLAIMERAlthough this material contains information of…

Documents Clinical Registries in Cardiac Surgery Peter S. Greene, MD CMIO, Johns Hopkins Medicine Diane Alejo....

Clinical Registries in Cardiac Surgery Peter S. Greene, MD CMIO, Johns Hopkins Medicine Diane Alejo Information Systems Manager Division of Cardiac Surgery September 15,…

Documents NCI NCCCP Pilot Launch Catholic Health Initiatives June 25-26, 2007 Presenters Debbi Honey, RN, MHA....

NCI NCCCP Pilot Launch Catholic Health Initiatives June 25-26, 2007 Presenters Debbi Honey, RN, MHA CHI Vice President Clinical Operations CHI liaison and contact for NCCCP…

Documents Clinical Registries in Cardiac Surgery

Johns Hopkins Medicine Clinical Registries in Cardiac Surgery Peter S. Greene, MD CMIO, Johns Hopkins Medicine Diane Alejo Information Systems Manager Division of Cardiac…

Documents Respiratory Therapy Department Data Considerations

Respiratory Therapy Department Data Considerations October 21, 2009 MMI â 405: HIT Integration, Interoperability, and Standards Suzi Birz, Nicki Cliffer, Lincoln Farnum,…

Documents Clinical Registries in Cardiac Surgery

Johns Hopkins Medicine Clinical Registries in Cardiac Surgery Peter S. Greene, MD CMIO, Johns Hopkins Medicine Diane Alejo Information Systems Manager Division of Cardiac…

Documents An Introduction to Site-Level Quality Management within the Clinical Research Process

NIDCR Serious Adverse Event Reporting System An Introduction to Site-Level Quality Management within the Clinical Research Process CROMS Clinical Research Operations and…

Documents Research

Research Compliance QUESTION 3 According to UMMC Policy, when must a clinical trial be registered at http://clinicaltrials.gov/ CLICK THE ACCURATE ANSWER A. At the end of…