uconn health

SCRO Contacts

Name Title Phone Email
Audrey R. Chapman, PhD Chair, SCRO Committee 860.679.1590 achapman@uchc.edu
Ellen Ciesielski SCRO Coordinator 860.679.6004 eciesielski@uchc.edu

 

SCRO Committee Members

Audrey R. Chapman, PhD, Committee Chair, Professor, School of Medicine, Public Health Sciences

Peter Barwick, MD, Physician (retired), Community Member

Eric Bernstein, JD, EdD, Associate Dean for Academic Affairs, School of Dental Medicine

Stephen Clark, PhD, Associate Professor Emeritus, School of Dental Medicine, Genetics and Genome Sciences

Caroline Dealy, PhD, Associate Professor, School of Dental Medicine, Craniofacial Sciences

Jaime Imitola, MD, Vice Chair of Research in Neurology, School of Medicine

James Mulrooney, PhD, Dean, Professor,  Central Connecticut State University, Biomolecular Science

Leonard Paplauskas, UConn Health, Associate Vice President, Research Administration (retired)

Ted Rasmussen, PhD, Associate Professor, UConn, Pharmaceutical Sciences

Ernst Reichenberger, PhD, Professor, School of Dental Medicine, Center for Regenerative Medicine and Skeletal Development

Richard Tombaugh, PhD, Theologian, Community Member

Isolde Bates, ex officio member, Business Services Manager, Genetics and Genome Sciences

Maureen Sansone, ex officio member, IRB Administrator, The Jackson Laboratory

Ellen Ciesielski, SCRO Coordinator, UConn Health, Research Integrity & Compliance

SCRO Policies, Regulations & Guidance

For a detailed description of UConn/UConn Health SCRO Committee policies, please consult the SCRO Policy Manual document.

 

For additional resources, please check out the following links:

Training for Users of Stem Cells

University policy requires all researchers and research staff, including students, post-docs, visitors, and faculty, to pass the Human Stem Cell Compliance tutorial quiz with 100% accuracy prior to engaging in research. The tutorial is intended to educate researchers on ethical issues associated with hESC and hiPSC research and inform them of relevant institutional, state, and federal policies and procedures.

 

The tutorial is not required for those conducting in vitro human induced pluripotent stem cell (hiPSC) research involving the generation of gametes, embryos, or other totipotent cells. The tutorial is also not required for research that requires SCRO review to secure State of Connecticut funding but otherwise would not fall under SCRO’s jurisdiction (i.e., non-human stem cells, etc.). All other research requires that research staff complete the tutorial prior to beginning work on approved SCRO projects.

 

To access the tutorial, quiz, and the sheet to record your answers, click on the links below. Return your answer sheet to SCRO Coordinator, Ellen Ciesielski, eciesielski@uchc.edu. You will be notified of your quiz results and receive a certificate upon successful completion.

Institutional Biosafety Committee Meeting Dates

The UConn Health Institutional Biosafety Committee (IBC) is federally mandated to review work with recombinant or synthetic nucleic acids.

This committee meets monthly, usually on the second Thursday of the month. Exceptions are noted (*). Receive forms from and submit to ibc@uchc.edu by the submission deadline.

Upcoming meetings 2023:

Date Time Location Submission Deadline
October 10, 2024 3:10 pm WebEx October 1, 2024
November 14, 2024 3:10 pm WebEx November 5, 2024
December 12, 2024 3:10 pm WebEx December 3, 2024
January 9, 2025 3:10 pm WebEx December 31, 2024
February 13, 2025 3:10 pm WebEx February 4, 2025
March 13, 2025 3:10 pm WebEx March 4, 2025
April 10, 2025 3:10 pm WebEx April 1, 2025
May 8, 2025 3:10 pm WebEx April 29, 2025
June 12, 2025 3:10 pm WebEx June 3, 2025
July 10, 2025 3:10 pm WebEx July 1, 2025
August 14, 2025 3:10 pm WebEx August 5, 2025
September 11, 2025 3:10 pm WebEx September 2, 2025
October 9, 2025 3:10 pm WebEx September 30, 2025

 

If you are a person interested in or concerned about this type of research, you are invited to attend a meeting of the UCONN Health IBC. Meetings will be held virtually for the foreseeable future. Please contact IBC@uchc.edu for more information.

WCG Institutional Biosafety Committee Services periodically convenes open meetings regarding a human gene transfer study at UCONN Health. Announcements about these meetings will appear below when they are scheduled.

 

 

 

What If I’m Doing Exempt or Non-exempt Recombinant or Synthetic Nucleic Acids (r/s NA) Experiments?

This page gives you some facts and a strategy for what you need to do about compliance when working with rDNA.

FACTS
  • If you will be working with rDNA and funded by NIH or working at an Institution where work involving rDNA is funded by NIH (like it is at UConn Health), you are working under the NIH Guidelines for Research Involving Recombinant or Synthetic DNA Molecules (NIH r/s NA Guidelines). Compliance to these guidelines is required as a condition of NIH funding (and that of many other agencies) for research involving rDNA at the whole institution.
  • Institutions (UConn Health), Institutional Biosafety Committees (IBCs) and Principal Investigators (PIs) are all responsible for compliance under the NIH rDNA Guidelines.
  • All faculty are required to take the IBC/DURC/Biosafety training available at the CITI training site every three years. Contact the BioSafety Program Coordinator to get instructions how to do this.
  • Many rDNA experiments are exempt to the NIH r/s NA Guidelines, but some that you might think are exempt may not be. Experiments that are not exempt need to be registered with the IBC before they are started. In some cases the application needs only to be submitted and accepted by the IBC before work may start.
  • Viral Vector rDNA experiments need to be registered with the IBC.
STRATEGY (What to Do and Not Do)
  • Determine if your experiment or set of experiments is exempt or not exempt.
  • If you know your experiment(s) is not exempt, contact the BioSafety Program Coordinator to begin the registration process.
  • Even if you believe your experiment(s) is exempt (or safe or used elsewhere), please contact the BioSafety Program Coordinator. The only way for a PI to be sure they have done all they can to ensure their compliance with the NIH r/s NA Guidelines, is for the IBC to determine that the PI’s experiment is exempt and document it. Fortunately, the BSO may serve as the IBC’s proxy to make this determination and perform the documentation. This makes the decision about whether an experiment needs to be registered or not, quicker and not too hard.
  • Do not begin any rDNA work without UCH IBC authorization or determination that the work is exempt by the BSO.

 

 Additional information regarding the IBC and r/s NA experiments

IBC Contacts

Please direct all submissions to the BioSafety Program Coordinator.

Name Title Phone Email
TBD Biological Safety Officer
Victoria Scranton BioSafety Program Coordinator 860.679.7533 vscranton@uchc.edu
TBD Director of Research Compliance–Animal Research & Safety

 

 

 

IBC Forms

Please contact the BioSafety Program Coordinator for all IBC forms.

For Chemical or Biosafety Animal Safety Protocols create a protocol in InfoEd. The forms for this are listed there.

Biosafety Policies, Regulations & Guidelines

Institutions that receive NIH funding for any research involving recombinant or synthetic nucleic acids must comply with the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules (NIH r/s NA Guidelines). Here at UCH, we commonly abbreviate this title to NIH r/s NA Guidelines.  You can read the full document.

The state of Connecticut has pertinent laws as well. Please see the CT Public Health Code 19a-36-A and the Requirements for Institutions with BSL-3 Facilities for more information.

The Biosafety in Microbiological and Biomedical Laboratories (BMBL), published by the CDC’s Office of Safety, Health, and Environment in conjuction with the NIH, is considered the national standard to promote the safety and health of laboratory workers. It covers the basic principles of biosafety, biocontainment, and provides detailed information on working safely with various pathogens, toxins, and other biohazards. Please take the time to review the BMBL and promote a culture of safety in your laboratory.

For those who may be in contact with human blood, body fluids or tissues, Bloodborne Pathogen training is a legal requirement (OSHA). For those interested in the specifics: