Congratulations to the Most Recent Awarded Grants to CSUEB:
Harassment: National Science Foundation has released its Federal Register notice on Reporting Requirements Regarding Findings of SexualHarassment, Other Forms of Harassment, or Sexual Assault. NSF has developed a new award term and condition that will require grantee organizations to report findings of sexual harassment, or any other kind of harassment regarding a PI or co/PI or any other grant personnel. The award term and condition also will require the grantee to report the placement of the PI or co-PI on administrative leave relating to a harassment finding or investigation." https://www.nsf.gov/pubs/issuances/in144.jsp
Data Sharing: Investigators are expected to share with other researchers, at no more than incremental cost and within a reasonable time, the primary data, samples, physical collections and other supporting materials created or gathered in the course of work. https://www.nsf.gov/bfa/dias/policy/dmp.jsp
IRB: Common Rule: Institutions are allowed to employ three provisions from the revised Common Rule (2018 requirements) (HHS 2018b).
Institutions that transition ongoing research studies to the 2018 requirements during the delay period must document and date their determination (HHS 2018b). The research that is transitioned must also fully comply with all of the 2018 requirements beginning on the general compliance date (21 January 2019).
The revised Common Rule requires that for any clinical trial conducted or supported by a Common Rule department or agency, one consent form be posted on a publicly available federal website within a specific time frame. The consent form must have been used in enrolling participants in order to satisfy this new provision.
At this time, two publicly available federal websites that will satisfy the consent form posting requirement, as required by the revised Common Rule, have been identified: ClinicalTrials.gov and a docket folder on Regulations.gov (Docket ID: HHS-OPHS-2018-0021). Additional federal websites that would satisfy the revised Common Rule’s clinical trial consent form posting requirement might be identified in the future.
At the end of every January is the due date for the mid-year Compliance Reporting. These include Cost Matching/Share Reporting, Subrecipient Monitoring, Centers and Institute Report, Conflict of Interest, etc
See the research of the faculty and student. Once a year, the researcher can present his or her work in poster format to the campus community. Tuesday is the faculty poster session. Wednesday is the student poster sessions. Also, the 10 students going to the statewide research competition presenting their oral presentations.
At the end of every July is the due date for the end of the year Compliance Reporting. These include Cost Matching/Share Reporting, Subrecipient Monitoring, Centers and Institute Report, Conflict of Interest, etc