February 2024 Newsletter
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Stay up-to-date with the latest news and resources from the Office of Research Protections (ORP)
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ORP Celebrates 25 Years!!
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This year, ORP is proud to celebrate its 25th anniversary!
Initially launched in 1999 as the Research Conduct and Compliance Office, ORP has evolved and expanded over the years to accommodate the needs of faculty and investigators and to facilitate research that meets the highest of ethical standards.
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Leaving Pitt, whether you are retiring or transitioning to another university, entails various complexities. From decommissioning labs to ensuring data retention and transferring grants, there's much to manage. But fret not, we're here to support you!
If you're departing from Pitt, please consult our Checklist for Investigators Leaving the University.
By filling out this online form, you'll also notify pertinent offices of your departure, prompting them to reach out with necessary information.
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Annual Disclosure Period Begins March 18
The University's Annual Disclosure Period begins on March 18. Disclosure forms are due by April 15.
If you are required to submit an annual disclosure, you will receive an email notification from MyDisclosures between March 18 and March 20.
Do not complete your annual disclosure until you receive the email notification from MyDisclosures! Disclosures completed before March 18, 2024 do not satisfy the 2024 annual disclosure requirement.
Training videos for disclosers, supervisors and administrators are available here. Step-by-step instructions on how to complete disclosures, supervisor reviews and access MyDisclosures reports are available here. Guidance regarding disclosure requirements is available here.
If you have questions, please contact ORP's Conflict of Interest Division at mydisclosures_support@pitt.edu.
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ORP oversees the Controlled Substance Guidelines for the University, assisting investigators in adhering to regulations set forth by the Drug Enforcement Administration (DEA). These guidelines outline the necessary protocols for obtaining, storing, and disposing of controlled substances. Additionally, they detail the mandatory background checks for laboratory personnel handling any amount of controlled substances.
If you use controlled substances in your laboratory, please be familiar with the Controlled Substance Guidelines.
If you have any questions about these guidelines, submit them through the ORP Support Request Form.
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Research!America Survey Shows Bipartisan Consensus on Importance of Medical Progress
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For over 30 years, Research!America has commissioned public opinion surveys to understand Americans’ views on medical, health and scientific research.
In January 2024, the advocacy alliance published a national survey that found that the majority of Americans—regardless of political affiliation—are more likely to support candidates who favor investing in medical and health research.
Key findings from the survey include:
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84% say it is important for political candidates to promote faster medical progress.
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69% of Americans are more likely to support a candidate if they favor increased spending on medical and health research.
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Americans say cost of healthcare is the most important health issue, followed by mental health and cancer.
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Monday, March 4, 2024
1:30 - 2:15 p.m.
Please join us for an introduction to REDCap, a secure web-based application designed to optimize clinical trial data collection. ORP's Education and Compliance Support for Human Subject Research (ECS-HSR) division, in conjunction with Health Sciences Information Technology (HSIT), will provide the rationale for implementation, a brief overview of the process, and plans for moving forward. There will be an opportunity for questions at the end of the session. The recording will be posted on our webpage and the slides provided to attendees.
Important: Use of the validated instance of REDCap is limited to those conducting research under a faculty held Investigational New Drug Application (IND) or Investigational Device Exemption (IDE) and is required for new research studies submitted to the FDA after January 1, 2024.
Register here.
Zoom link will be provided by e-mail upon registration.
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Need help in ensuring that your research meets regulatory requirements and ethical standards?
Then use the ORP Support Service!
Just answer a few questions and we will put you in touch with the right professionals to help facilitate your research.
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