DATE

 

TOPIC

 

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6/20/06

New IRB SOP's

Powerpoint presentation not yet available

4/11/06

Environmental Health & Safety, Radiation Safety and the Institutional Review Board:

Bringing Them All Together

Powerpoint presentation not yet available

3/14/06

Change Management in Research Administration: An Operations and Systems Approach

n/a

2/14/06

Discussion with Research Personnel: Perspectives on the IRB Process

Powerpoint presentation not yet available

1/17/06

Human Subjects Research

at Columbia University

Powerpoint presentation not yet available

12/13/05

RASCAL User Manuals: 

IRB (Version II) and HIPAA

Powerpoint presentation not yet available

11/29/05

Accreditation of the Columbia University

Human Research Protection Program

Powerpoint presentation not yet available

10/11/05

IRB Frequently Asked Questions

Powerpoint

Collaborative Research

Handout

Changes in NIH PHS 398

&

Certificates of Confidentiality: How, When & Why

Powerpoint

9/15/05

Noncompliance

Powerpoint

8/16/05

International Research

Powerpoint

Ethical Research in an Unequal World

Powerpoint

7/21/05

Emergency Use, Compassionate Use,

and Emergency Research

Powerpoint

6/23/05

Research with Children:

Requirements for IRB Review

Powerpoint

5/10/05

FDA Regulated

Research

Data Monitoring Committee Establishment and Management

Powerpoint

Special Topics in IND Regulation

Powerpoint

4/12/05

Ask the IRB:

Question & Answer Session

(IRB Reviewer Form)

Word Document

3/15/05

HIPAA Privacy Standards

& Electronic Data Security

Powerpoint

2/15/05

Renewing an IRB-Approved Protocol

Powerpoint

1/18/05

Status of the IRB

Powerpoint

11/09/04

Research Use of Stored Data and Tissues

Powerpoint

 

(Data & Tissue Repositories)

Word Document

10/12/04

Who Ultimately Protects Human Research Subjects?

Powerpoint

9/14/04

Research at Non-CU Sites

Powerpoint

8/17/04

Collaborative Research

Word Document

7/29/04

Ask the IRB:

Question & Answer Session

Questions

from the floor

5/18/04

Research Billing Compliance

Powerpoint

4/13/04

Adverse Event Reporting Policy

Powerpoint

3/09/04

Review of Research

Using Human Specimens

Powerpoint

 

Word Document

(IRB Terminology)

 

Word Document

(IRB Review of Research)

2/10/04

Facilitating Efficient IRB Review

Part II: Informed Consent

Powerpoint

1/13/04

Facilitating Efficient IRB Review

Part I: Preparing Submissions

Powerpoint

 

Word Document

 

12/09/03

Research at Columbia University

Education Training Overview

Powerpoint

11/11/03

Human Subjects Research

at Columbia University

Powerpoint presentation not currently available