Pitt Research
Office of Research Protections

Restrictions on Malign Foreign Talent Recruitment Programs Increase

The CHIPS and Science Act of 2022 requires that key personnel certify that they are not part of a Malign Foreign Talent Recruitment Program (MFTRP) at the time a proposal is submitted to a federal funding agency or annually thereafter for the duration of the award. Federal agencies have begun to implement this certification through the use of new common disclosure forms for the Biographical Sketch and Current and Pending (Other) Support

The federal government's definition of a MFTRP is long and can be confusing. The Office of Research Security and Trade Compliance has a new section on their website that contains helpful information about foreign talent recruitment programs, including the federal definition of a malign program. Faculty who suspect they may have been contacted by or become associated with an MFTRP are encouraged to contact Researchsecurity@pitt.edu or Allen A. DiPalma at dipalma@pitt.edu.

Requirements for Consulting and Outside Activities


University members are encouraged to consult for or advise companies, provided they obtain prior approval from their supervisors and adhere to all applicable University policies.

Before you enter into a consulting, advisor, or other new relationship with any outside entity, follow the steps outlined on the Outside Activities – Consulting page of the Conflict of Interest (COI) Division website. These steps must be followed prior to signing a new consulting, advising or other agreement and prior to initiating a new consulting or other outside activity. If you have questions, please contact the COI Division at coi@pitt.edu.

Department of Health and Human Services Updates Research Integrity Policy with New Rules

In response to growing concern about research integrity, the Department of Health and Human Services has updated its Research Integrity Policy with new rules on how universities should investigate claims of research misconduct.

The new federal rules, which apply to all U.S. Public Health Service-funded research, aim to streamline the inquiry process and re-assert standards that must be followed when investigating research misconduct. Further, the rules provide institutions with the clarity, flexibility, and transparency needed to efficiently investigate and resolve claims. The University is reviewing the new regulations and will work to update our Research Integrity Policy by the compliance date of January 1, 2026.

Telling the Story of Animal Research at Pitt


animalresearch.pitt.edu

Animal research remains a critical component of our research enterprise, and achievements in this realm have resulted in scientific breakthroughs and life-saving advancements in medicine. We have the opportunity to tell the story of animal research at Pitt on a dedicated site maintained by the University, animalresearch.pitt.edu.  

We are actively seeking new submissions for this site.  If you have noteworthy stories to share related to the impact of your animal research, please submit them to Dr. Bill Yates, Vice Chancellor for Research Protections, at vcorp@pitt.edu.

Fall Semi-Annual Facility and Lab Space Reviews

Federal regulations require that the Institutional Animal Care and Use Committee (IACUC) inspect, at least once every six months, all of the University's animal research sites using the Guide for the Care and Use of Laboratory Animals and other regulatory documents as a basis for the evaluation.

Inspections of animal housing and use sites are currently underway. To prepare for the review of  your animal use space, we encourage you to watch the video titled, “What to Expect When You Are Expecting a Review of Your IACUC-Approved Space & Animal-Related Activities.” 

Supporting Human Subject Research through Reliance Services


Since 2020, the revised Common Rule (45 CFR 46.114) has mandated that cooperative research projects involving more than one U.S. institution must rely on a single Institutional Review Board (IRB) for the portion of the research conducted in the United States. ORP's Human Research Protection division is committed to supporting multi-site human subject research through our Single IRB (sIRB) Reliance services.

We recognize that navigating IRB Reliance can be complex, and we are here to provide assistance. Whether you are seeking for Pitt to serve as the IRB of Record for non-Pitt collaborators, or if another IRB will take on that responsibility, specific requirements must be met for submitting such requests. For more information and detailed step-by-step instructions, visit the "Reliance Guidance" section of our website.

Explore ORP's Customized Onboarding Process

ORP is here to assist new University members jumpstart their research through our customized onboarding process. These onboarding sessions provide individualized assistance in protocol writing and regulatory compliance, while also establishing a point-of-contact that is helpful in addressing questions in the future.

New investigators have indicated that these personalized meetings are highly useful. If you are interested in our onboarding services, please complete this short survey so we can determine your needs. Visit our site to learn more.

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