News
Beginning Monday, April 11th, all new protocol submissions, modifications, adverse events, violations and continuation reviews may be submitted electronically. This is an initial step in the shift from paper to electronic submission as the web-based E-IRB program is being developed.
With the assistance of the UKHC Business Partners, we are pleased to make available a college-level version of the monthly PI Report. Using the versions of the report that the SRAS receives by CGO and IBU, this is a college-wide report that can be easily filtered by department. We have posted the report using February data to the College’s Finance SharePoint site (accessible to chairs and DAs; in the Grants Reports folder, see SPA PI Reports folder) and also to the shared IBU FI drive (in the ! WBS Elements folder, see !
The University of Kentucky Department of Biological Safety would like to invite you to register for the following seminar:
By March 25, 2016, NIH will release the new FORMS D packet to accommodate the updated requirements for applications due on or after May 25, 2016.
The changes in the new FORMS D packet focus on the following areas:
The deadline to submit an abstract for the CCTS Spring Conference and cooperating conferences has been extended (for most sessions*) to Friday, April 1, 2016.
When you ask Brett Spear about what he most admires in his wife and colleague, Martha Peterson, a smile instantly appears on his face.
The pair, both professors in the University of Kentucky College of Medicine Department ofMicrobiology, Immunology and Molecular Genetics, has been married for 32 years and has two sons. Yet, because they have different last names, not everyone on campus recognizes their connection.
OSPA recently published instructions allowing PIs to track their own eIAFs. To access the instructions, follow the link below.
http://www.research.uky.edu/ospa/info/docs/OSPA%20PI%20Tracking%20Report%20Instructions.pdf
NIH is now requiring grant applicants to validate key reagents to be used in the proposed research, particularly cell lines. Major journals are also starting to require such validation for publication. The preferred validation method is STR (short tandem repeat) profiling. Commercial firms provide this service for fees ranging from $70 to $300, depending on the firm and the precise work being done.
Beginning March 25, 2016, the website Grants.NIH.gov will be transformed into a more helpful and usable site. NIH has used input from surveys, reviews and discussion panels to create a more streamlined site with less clutter and more context. The new site will offer a new homepage, an updated forms page and improved details on how to apply.
To access the NIH site, click here.
The purpose of the Research Enrichment Program (REP) is to stimulate new research and support existing research and scholarly activities within units (departments, centers, and institutes), thus supporting the university's strategic objective of facilitating interdisciplinary research and collaborative scholarship. The REP funds will be awarded to units according to the percentage distribution indicated in Item #8 on the eIAF.
As a reminder, the University of Kentucky defines an investigator in the Administrative Regulations 7:2 as, “project director or principal investigator/program director, co-investigator, collaborator, senior/key personnel, faculty associate, and any other person, regardless of title or position, who is responsible for the design, conduct, reporting, or proposing of research or other activity that is sponsored by an extramural agency.” Investigators also include “other significant contributors” and “sub-investigators.” All investigators on a sponsored project proposal should be included on t
From Zika to Ebola, the emerging viruses of the 21st century pose a threat to populations throughout the world as silent invaders of the human body. While viruses infect most people multiple times a year with varying degrees of severity and symptoms, no two viruses function in exactly the same way.
Clinical trial research is an important component of the academic activities at the University of Kentucky. The administrative issues related to the financial management of clinical trial research are challenging, but need to be addressed to facilitate efficiency and compliance. We have engaged Huron Consulting to provide a nationwide perspective on best practices on fiscal management of clinical trial research. Below is the provisional suggestion for the scope of the project:
All faculty in the College of Medicine (physicians and basic scientists) are required to participate in financial conflict of interest disclosures. The 2 types are disclosure are listed below: