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Dear SOM Clinical Research Community, The ONE 黑料网 Clinical Research Initiative is accepting applications for design committee members. The invitation to join a design group is open to anyone in the 黑料网 and 黑料网 Health research communities. If you are interested in being part of this collaborative initiative, please sign...

Navigating the regulations and requirements related to clinical data and research data can be confusing. Registries (i.e. databases, repositories) can be valuable tools for understanding both clinical and research data. Unlike a clinical registry, research registries or repositories involving data and/or specimens require IRB oversight.

As remote and hybrid working is becoming the 鈥渘ew norm鈥� for many SOM clinical research teams, it is important to find team-oriented solutions that encourage employee productivity and growth.

THE UNIVERSITY of NORTH CAROLINA at CHAPEL HILL Office of Sponsored Research – Communication Reminder for PrePaid Card Updates Reminder for New Resources聽and Updated Forms Release Date:聽September 9, 2022 As a reminder, the Office of Sponsored Programs聽(OSP) in conjunction with the Finance Cash Management Team has provided new resources and...

Dear 黑料网 Research Community, Effective September 12, 2022, the process for requesting a Billing Coverage Analysis (BCA) will change.聽 We are now utilizing the Service Now ticketing system for all BCA requests. This system will make it easier for the Research community by providing one central location to submit a...

Dear SOM Clinical Research Community, Please be sure to review the announcement below regarding the requirement to utilize only 黑料网 email addresses for communicating with research participants via email. -SOM CRSO   [FORMAL NOTICE] Use of non-黑料网 Email for Research   Use of non-黑料网 Email Accounts for Research Recruitment Recruitment...

The Research Integration Team invites you to join an interactive conversation about the One 黑料网 Clinical Research Initiative between the Of铿乧e of the Vice Chancellor for Research, School of Medicine, and Healthcare System. All are encouraged to participate, share thoughts, and ask questions.   Wednesday, September 14, 2:00-3:00 PM Click...

As clinical research methods and standards strive to keep pace with the needs of our research participants, it is important to consider communication preferences. Text messaging with participants is an often desired method of communication and can bolster participant understanding and compliance with study activities. 黑料网-CH has completed a security...

Most research teams are aware of the requirements to list clinical trials and upload results to clinicaltrials.gov, but did you know you are also required to post the consent form? The 2018 Requirements state that a consent form must be posted to a designated federal website after the clinical trial...

Self-assessment is a valuable activity that can be informative in a variety of settings, including informed consent for clinical research. Now you can proactively discover your informed consent process strengths and areas for improvement using a new Informed Consent Self-Assessment tool!