'Study documents' presentation slideshows

Preparing For A VA Compliance Audit

898 views • 36 slides

Source Documentation

Source Documentation. Catherine Gregor, MBA, CCRC, CCRP CRC Workshop August 1, 2014. Which of these Study Documents are considered Source documents?. Regulatory Binder Medical Record Case Report Form Participant File. 2. Source Data

426 views • 26 slides

Billing 3 rd Party Payors for Services as part of Clinical Research

Billing 3 rd Party Payors for Services as part of Clinical Research. Presented by OCRA to the Research Committee March 3, 2010. Background of CMS Clinical Trials Policy National Coverage Determination (NCD).

400 views • 24 slides

Undergraduate Advisory Board

Undergraduate Advisory Board. Industrial Engineering Program Department of Industrial and Manufacturing Engineering. Agenda. Overview of the Department (Ken Chelst) What is ABET? (Darin Ellis) Overview of Industrial Engineering Undergraduate Program (Darin Ellis) Discussion (All)

372 views • 24 slides

Partnering with Pharmaceutical Leaders Active in Clinical Research

Partnering with Pharmaceutical Leaders Active in Clinical Research. DO IT RIGHT THE FIRST TIME!. Company Overview. Berlin-based CRO Founded in 2004 Founding member of MEDIS RESEARCH GROUP Audited member of BVMA e.V. (in association with EUCROF) since 2009

315 views • 22 slides

Partnering with Pharmaceutical Leaders Active in Clinical Research

Partnering with Pharmaceutical Leaders Active in Clinical Research. DO IT RIGHT THE FIRST TIME!. Company Overview. Berlin-based CRO Founded in 2004 Founding member of MEDIS RESEARCH GROUP Audited member of BVMA e.V. (in association with EUCROF) since 2009

222 views • 22 slides

The Secret to Preparing Documents for a Smooth Approval Process

The Secret to Preparing Documents for a Smooth Approval Process. Research Compliance Administration Training Presentation Wednesday, July 18, 2007 Presenter: Heather Kemp, MBA Research Compliance Coordinator 278-7812 hkemp@iupui.edu.

270 views • 16 slides

Multi-Institutional Facilitated IRB Review

Multi-Institutional Facilitated IRB Review. Third Annual Clinical Research Management Workshop June 22, 2010. Kathleen Lawry, MSSA, CIP, CIM, Assistant Director Research Administration MetroHealth Medical Center. Philip A. Cola , MA

210 views • 10 slides

Multi-Institutional Facilitated IRB Review

Multi-Institutional Facilitated IRB Review. Third Annual Clinical Research Management Workshop June 22, 2010. Kathleen Lawry, MSSA, CIP, CIM, Assistant Director Research Administration MetroHealth Medical Center. Philip A. Cola , MA

194 views • 10 slides

Multi-Institutional Facilitated IRB Review

Multi-Institutional Facilitated IRB Review. Third Annual Clinical Research Management Workshop June 22, 2010. Kathleen Lawry, MSSA, CIP, CIM, Assistant Director Research Administration MetroHealth Medical Center. Philip A. Cola , MA

176 views • 10 slides

Investigator Meeting January 2010

Investigator Meeting January 2010. Protocol Review and Refresher. Study close out. Supplies Data EFIC Regulatory. Study close out - supplies. Destroy Remaining Study Drug Remove all study boxes from field Waste and retire study drug in WebDCU Remaining Supplies

225 views • 7 slides

INTRODUCTION

130 views • 1 slides

Curriculum and the CCSSM: Continued Conversation

Curriculum and the CCSSM: Continued Conversation. Just glancing at these sequenced units of study, what do I notice? What is the flow? What do I like? What are concerns? What questions do these raise ? How does each support the spirit of the CCSSM ?

124 views • 1 slides