Clinical Interface Core (CIC)

The following list of resources, while not exhaustive, provides you with information on how research works at UIC. The links offer both national and local standards, tools and contacts, to help answer your questions as you plan and conduct your research.

CCTS's Regulatory Support , Advocacy and Bioethics Core services
Study Coordinators Guide to Laboratory Testing
Environmental Health and Safety Office
Clinical PAF Processing Office
Cancer Center Protocol Review Committee
Office for the Protection of Research Subjects
OVCR
OVPAA
BRL
Center for Disease Control and Prevention
NIH Bioethics Resources on the Web
US FDA
Drugs and Biologics
Medical Devices
FDA Operations
Clinicaltrials.gov
VA

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Environmental Health and Safety Office:

BIOLOGICAL SAFETY
Biosafety Manual
Bloodborne Pathogen Program
Guidelines for Working with Bloodborne Pathogens
Disposal of Potentially Infectious Materials.
CHEMICAL SAFETY
Guidelines for Handling Simple Chemical Spills in Laboratories
ERGONOMICS
FIRE
GRANT SUPPORT
LABORATORY SAFETY
LAB MOVES
LASER SAFETY
Laser Safety Policy
OFFICE SAFETY
RADIATION SAFETY
STANDARDS, MANUALS, & GUIDELINES
TRAINING
Visitors Policy
Radiation Safety - Human Subject Research Policy
Chemicals of Interest for Department of Homeland Security
Benzene Policy
2007 CHEMICAL HYGIENE PLAN

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Clinical PAF Processing Office

Request for Use of University Hospitals and Clinics Services
Memorandum of Understanding
Grants and Contracts Registration Form
LINK Patient to Grant Account
Cover Sheet for Research Subject Requisition Forms
Transfer of Revenue or Expenditure Template(Sample)

Billing
Hospital Fee Policy

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Cancer Center Protocol Review Committee

Cancer Center Protocol Review Committee

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Office for the Protection of Research Subjects

Human and Embryonic Stem Cell (hES)
Education and Training
Informed Consent On-Line Tutorial
OPRS Policies and Guidance
On-line training opportunities in research
International Compilation of Human Subject Research Protections

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OVCR

Getting started with research:

Case Report Forms
Grant & Contract Proposals
Protocol Review: Human, ESCRO
IRB/OPRS Forms & Instructions
Protocol Review: Animal, rDNA, Infectious Agents
Animal Care Center (ACC) Forms
Funding Opportunities
Technology Transfer (Office of technology Management)
Illinois Ventures
Material Transfer Agreement
Academic Industry Relations
Responsible Conduct in Research: On-line Training and Certification

Selected Research-Related Policies:

Conflict of Commitment & Interest
COI Disclosure
Academic Integrity
Responsible Conduct in Research (RCR)
Addendum to Publication Agreements for CIC Authors

Grants and Contracts
Preparing Budgets
Receiving Awards
Export Control

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OVPAA

Conflicts of Commitment and Interest Policy
Policy Clarification Conflicts of Commitment and Interest in Teaching
Report of Non-University Activities (RNUA) Form
RNUA Explanation and Instructions
RNUA FAQ
Other VPAA Policies

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BRL

Biologic Resources Laboratory
Getting started with Animal Research

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Center for Disease Control and Prevention

Human Participant protection in CDC research

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NIH Bioethics Resources on the Web

NIH Bioethics links

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US FDA

Information sheet guidances *
Frequently Asked Questions (1998) *
Cooperative Research (1998)
Data Retention when Subjects Withdraw (2008)
IRB Information Sheets--Research and Review (Updated 9/98) -- Cooperative Research (1998)
Non-Local IRB Review (1998)
IRB Information Sheets--Research and Review (Updated 9/98) (1998)
Sponsor-Investigator-IRB Interrelationship (1998)
Foreign Clinical Studies, Acceptance of (2001)
Charging for Investigational Products (1998)
Recruiting Study Subjects (1998)
Payment to Research Subjects (1998)
Screening Tests Prior to Study Enrollment (1998)
Guide to Informed Consent (1998)
Use of Investigational Products When Subjects Enter a Second Institution (1998)
IRB Information Sheets - Updated 9/98
Exception from Informed Consent Requirements for Emergency Research (2011)
"Off-Label" and Investigational Use of Marketed Drugs, Biologics and Medical Devices (1998)
Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials (2008)
Regulatory Procedures Manual (2001)

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Drugs and Biologics

Emergency Use of an Investigational Drug or Biologic (1998)
Treatment Use of Investigational Drugs (1998)
Waiver of IRB Requirements for Drug and Biological Product Studies (2006)
Drug Study Designs (1998)
Evaluation of Gender Differences (1998)
Frequently Asked Questions - Statement of Investigator (Form FDA 1572) (2010)

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Medical Devices

Frequently Asked Questions about IRB Review of Medical Devices (PDF - 105KB) (2006)
Significant Risk and Nonsignificant Risk Medical Device Studies (PDF - 121KB) (2006)

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FDA Operations

FDA Institutional Review Board Inspections (PDF - 45KB) (2006)
FDA Inspections of Clinical Investigators (PDF - 48KB) (2006)
Clinical Investigator Administrative Actions - Disqualification (2010)
Running Clinical Trials

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Clinicaltrials.gov

PRS information

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VA

VA Office of Research & Development
Office of Research Oversight
Research at Jesse Brown VA Medical Center

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