PPT-Event Repository Reporting

Mark Hawkins ACACSO May 11 13 2016 2 Idaho History Event Lifecycle Dependencies Idaho Originally included in the Washington territory and included Montana amp Wyoming George M Willing Shoshone the sun comes from the mountains . difficile LabID Event FacWideIN January 2013 Healthcare Personnel Influenza Vaccination All Inpatient Healthcare Personnel January 2013 Medicare Beneficiary Number All Medicare Patients Reported into NHSN July 2014 CLABSI Adult Pediatric Medical Su HANDBOOK FOR REPORTING NASDA Q CLEARING DATE: 201 4 - 11 - 07 DOCUMENT VERSION : 2. 2 LEGAL DISCLAIMER The content of this document is subject to change without notice. Nasdaq makes no representati and . Associate Responsibilities for . SafeCare. General Orientation. Objectives for Risk General Orientation. Teach you how to respond and report safety . concerns and . events. Event Reporting . What. Phil Brammer. Phil Brammer. Over 10 years’ experience in database technologies, data warehousing, ETL, on-call…. Started on Red Brick Data Warehouse. Ralph Kimball’s product. . Inmon. Who?. Worked with Teradata at PayPal. Lisa Mably. lisa.a.mably.civ@mail.mil. 2. Agenda. Sustainment Reporting. Sustainment Reporting Overview. Contractor Cost Data. Future CSDR Co-Plan. Technical Data Reporting (TDR). Description. TDR Examples. Simplified process. Electronic submission to IRB. “Robust” guidance from HSO. One reporting mechanism (no separate forms). New 60 day amendment submission deadline. IRB Makes the Determination. When . AIRS – Anesthesia Incident Reporting System. Patrick Guffey MD. Chair, AQI AIRS Steering Committee. Richard Dutton MD MBA. Chief Quality Officer, AQI. Lance Mueller. Director, AQI. June 26, 2014. Insights. Allison Murad, MPH. Surveillance for Healthcare-Associated and Resistant Pathogens (SHARP) Unit. Michigan Department of Health and Human Services (MDHHS). Why NHSN?. The “Gold Standard” for HAI Reporting and . Acknowledgement. Acknowledgment to . Ms. Chun Geok Ying . for preparation of the core contents of this presentation. Outline. Why is safety practices important?. What is safety monitoring? . Safety Reporting. Incident Time in 24-hour format Report DateReported by Address Speci31c area where incident occurred Incident Address Was an Agency or Authority Noti31ed Yes Adventure/Program/Event Gen Human Research Protection Program (HRPP). HRPP COMPLIANCE AND QUALITY TEAM . Yale University. . Federal regulations (45 CFR 46 & 21 CFR 56) require institutions to establish written procedures for ensuring prompt reporting of any unanticipated problems involving risks to subjects or others (UPIRSOs) to the IRB, appropriate institutional officials, and the federal department or agency head.. Version 04 . Feb. 2021. In . this. . training course you will learn. What. is . pharmacovigilance. ?. What is the pharmacovigilance responsibility of the investigator in a clinical trial?. What is the pharmacovigilance responsibility of the sponsor in a clinical trial?. 2019 Spring. SAFETY of the SUBJECT. Safety of the Subject. Key definitions. Identifying, documenting and reporting. Investigator reporting responsibilities . How are research participants protected? . �� &#x/Att;¬he; [/;ott;&#xom ];&#x/BBo;&#xx [6;.44;i 3;.73; 8;.68;– 4; .76;& ];&#x/Sub;&#xtype;&#x /Fo;&#xoter;&#x /Ty;&#xpe /;&#xPagi;&#xnati