Chicken Soup for the Busy Coordinator Chicken Soup for the Busy Coordinator May 2009.

Slides:



Advertisements
Similar presentations
Chiari Surgical Outcomes Trial PI: Bermans J. Iskandar and Timothy George with collaboration from John Kestle ASAP-funded pilot study ASAP-funded pilot.
Advertisements

University Research Procedures Research Processing Training Day - 28 April 2006.
Chicken Soup for the Busy Coordinator B2B Research Online Portal FAQs
Chicken Soup for the Busy Coordinator
Chicken Soup for the Busy Coordinator
USC Clinical Trials Office (CTO) Answers to CTOs who, what, when, and how questions Soheil Jadali Director, Clinical Trial Office.
Chicken Soup for the Busy Coordinator September 2009.
Building A Clinical Trial Budget The Vanderbilt Way Lynda Lane, MS, RN Administrative Director, GCRC.
The Principal Investigator’s Roles and Responsibilities Chicken Soup for the Busy Coordinator (May 2010)
HOT TOPICS ARCHIVING OR HOW NOT TO DUMP YOUR RUBBISH!
Chicken Soup for the Busy Coordinator Aug Scenario: Aim: Randomised, double-blind, phase III clinical trial to compare the safety and efficacy of.
The Early Phase (0-I-II) Clinical Drug Research Unit of Maastricht University Medical Center (MUMC) prof dr L. Van Bortel Drug Research Unit Maastricht.
My Sponsor Wants to Know if I Can Use a Central IRB An Introduction to Using a Central/Commercial IRB at MSSM.
Subcontracts 101 By Mitali Ravindrakumar USC Collaboration between Parties Perform Subcontractor Analysis Sponsor - Fund Project/Subcontr act Negotiate.
Chicken Soup for the Busy Coordinator February 2009.
Good Clinical Practice in Research
Chicken Soup for the Busy Coordinator Dearest colleagues, friends and members of the Clinical Research Coordinator Society, Welcome to the launch of the.
Regulatory Submission Process  Clinical Study Application: 1. Submit an appointment requestappointment request 2. Fill one of the three templates: - BE.
B2B Research Online Portal FAQs Chicken Soup for the Busy Coordinator (February 2010)
Chicken Soup for the Busy Coordinator October 2009.
Chicken Soup for the Busy Coordinator March 2009.
Good Clinical Practices Regulatory Guidelines for the Conduct of Clinical research Introduction to Research Pharmacy Services Javier Palacios, R.Ph. Sponsored.
Liability in Clinical Research Clinical Effectiveness Unit Division, PS & MD 2005 Liability in Clinical Research Clinical Effectiveness Unit Division,
Chicken Soup for the Busy Coordinator Nov 2010 PROTOCOL FEASIBILITY.
Study Team Members and Responsibilities Chicken Soup for the Busy Coordinator (April 2010)
Principal Investigator C hicken S oup for the B usy C oordinator (October 2010]
Legal Aspects of Clinical Trials Shekhar Potkar Director Clinical Research Pfizer Limited.
Indemnify Compensation for damage, loss, or injury suffered. Insure someone against legal responsibility for their actions.
Are IRBs Efficient, Effective, or Redundant? David C. Clark, Ph.D. Director, Research Compliance Rush University Center.
The Contracting Process (Why Does it Take So Long?) Libby Salberg, Associate Director Beth Watkins, Contract Analyst, Team Manager Janet Fry, Manager Clinical.
Andrew Thornton, Chairman, RAH HREC
New online DSRB Supplementary Report Forms Chicken Soup for the Busy Coordinator (January 2010)
Driving Innovation to Market. Partnering with the Office of Intellectual Property and Industry Sponsored Research December 10, 2013 Tara A. Kamin, Esq.
Office of Clinical Research and Innovative Care Compliance (OCRICC) What You Need To Know About Conducting Research at Froedtert Hospital Roberta Navarro,
NOVEMBER 13, 2012 SERIES 2, SESSION XI OF APPLICANTS & ADMINISTRATORS PREAWARD LUNCHEON SERIES Research Sponsored by Industry – Putting an Agreement in.
CLINICAL RESEARCH STUDIES Janette Hannam, MS, CTRA Asst. Director for Research, OSP.
February 12, 2014 Non-CISO Non-CTU Studies: How They Differ.
Budget Development Presented by: Jean Mercer Associate Director for Clinical Research Administration Office of Clinical Research – School of Medicine.
How to Successfully Apply to the IRB Richard Gordin, IRB Chair True Rubal, Administrator / Director For the Protection of Human Participants in Research.
IWK Research Ethics - Workshop Series Session #2 REB Review Procedures How to submit … October 24, 2013 Bev White, Manager, Research Ethics Research Services,
NCURA April 25, 2006 Compliance Coordination and Research Administrators: Opening the Lines of Communication Judy Harris, Assistant Director, Arizona State.
Chicken Soup for the Busy Coordinator April 2009.
LETTER OF INTENT FOR INDUSTRY SPONSORED RESEARCH Signe Denmark, SCTR Research Opportunities & Collaborations Ryan Mulligan, SCTR Grants & Contracts Navigator.
Chapter 71 Data Ethics. Chapter 72 Thought Question 1 Many new treatments for rapidly lethal diseases offer very little or no benefit to patients. Thus,
Module C FDA Regulations Regulatory Documents Patricia E. Koziol 1Module C Final Version 10-apr-2010.
Business Operations Pre-Award. What is required to begin the business process? Possible indicators CDA executed Cancer Center MDG/PRC approvals Department.
Partnering With Industry for Clinical Research Luke Lin, MD, and Ralf Schnall.
Chicken Soup for the Busy Coordinator July Question: My trial has completed and we are preparing for closure of study. How long do we need to archive.
Audit – Consultation – Ethics & Compliance – Enterprise Risk Management – Investigations Office of Internal Audit and Compliance Best Practices for Protecting.
Vice Chancellor for Institutional Compliance Robert Bishop, (501) , University Hospital Compliance Officer Jane.
Ensures that studies are billed for research specific procedures.
HA Central Register of Clinical Research 1 Dec 04 HA REC.
Using Australian Clinical Sites – Challenges for International Sponsors Prof A J (Tony) Webber Clinical Network Services Pty Ltd Brisbane, Australia.
Research Foundation Insurance 101 Learning Objectives Participants will understand: The Research Foundation’s Insurance Program and Coverage The RF Insurance.
Business Operations Pre-Award. Confidential Disclosure Agreements (CDA)/ Non-Disclosure Agreements (NDA)
The IOM Template Project: Material Transfer Agreements and Clinical Trial Agreements Presentation to the IOM Forum on Drug Discovery, Development and Translation.
Responsibilities of Sponsor, Investigator and Monitor
Clinical Trial Billing and Patient Remuneration
Responsibilities of Sponsor, Investigator and Monitor
Introduction to Clinical Trials: Documents and Processes
Office of Research Administration: Clinical Research Contracting
Clinical Trial Contracts Office -What’s the Hold Up?
Introduction to Sponsored Programs
Agreements OSR Symposium
Industry Funded Research - Process for Contracts
Clinical Trials at USC – Who handles budgeting and contracting?
PROCESSING SPONSORED PROPOSALS AT THE JOHN F
Good Clinical Practice in Research
Contracting Considerations in Research & Innovation
S A Overarching SOPs Funding Secured Training Records
Presentation transcript:

Chicken Soup for the Busy Coordinator Chicken Soup for the Busy Coordinator May 2009

Tip of the Month Case Scenario: I have a new clinical trial agreement that is in the process of negotiation. For ethical reasons and safety of the subjects, insurance and indemnity will have to be provided for this study. Who should be the one providing insurance coverage and indemnity for this study?

Answer The party to provide the insurance coverage and indemnity for the clinical trial, will be based on the type of trial being conducted: –For an Industry Sponsored Trial, insurance and indemnity will be provided by the Company sponsoring the trial. –For the Principal Investigator initiated Trial, insurance will be provided by the institution that undertakes the trial. The provider of the study material will provide the indemnity for the product that is used in the clinical trial. (Exception is when study material are commercially available, and given according to labeled use and dosage.) The certificate of insurance is to be provided by the Sponsor/ Clinical Research Administration office of the institution.

Clinical Trial Agreement (CTA) –Clause on “Indemnity” –Clause on “Insurance” PCR SOP 501-B02 PCR NHG CTA Guidelines PCR NHG CTA Checklist PCR NHG CTA Template SGGCP 5.8, 8.2.4, 8.2.5, References

Feedback Your feedback is important to us. Do write to us through: Snail mail: Clinical Research Coordinator Society (CRCS) c/o Research & Development Office 6 Commonwealth Lane #04-01/02 GMTI Building Singapore