Upenn Data Use Agreement
Category : Uncategorized
The senior auditor must be a faculty member or principal investigator, but students may sometimes have access to the data as research staff as part of the agreement. This site provides instructions on the different types of agreements that are often used in research on human issues at Penn. Please note that some of these agreements require evaluation by offices outside the IRB. Patrick Stanko is the IRB`s main interlocutor on general issues relating to agreements. However, DUAs may also include a data provider`s requirements to process unregulated, unidentified or other low-risk data. Interpretation of terms and conditions of sale and other data variables should be left at appropriate offices within the university. You are not expected to be an expert in contract interpretation. CHOP IRB has had a Master Reliance Agreement with the University of Pennsylvania since 2005. The last agreement was executed on 5 December 2016.
Hundreds of studies have been included in the agreement, which benefits both IRBs and reduces the burden on CHOP and Penn investigators. A Data Use Agreement (DUA) is a legally binding agreement that targets at least the data, the CONDITIONS AND THE CONDITIONS OF THE DATA AND THE RIGHTS OF THE PARTIES with regard to the use of data at least TROP DEFINE. A limited set of data excludes any information on protected health (PHI), with the exception of the following information: (1) date and (2) geographic information at the postcode, city or city level. The contract application and data entry form will be reviewed by Penn State to determine the next steps needed to approve the terms and conditions on behalf of Penn State. Step 3: What kind of safe technology and workspace are needed to use the data? The Master Common Reliance Agreement determination form should be completed by THE ORGANISME on the IRB Audit website, signed by the IRB REPRESENTATIVE of PI, and then forwarded to each relying site for institutional approval and signature. Since May 25, 2017, the NIH has required all national sites participating in multi-center research studies (where each site performs the same protocol) to use a single IRB (sIRB). The final NIH Directive on the use of a single institutional multi-site research review committee applies to research without any exempt human subject, whether supported by grants, cooperation agreements, contracts or the NIH Intramural Research Program. It does not apply to professional development, research training or scholarships.
This directive applies to all competing grant applications (new, renewed, revised or reinstalled) with receipt dates on May 25, 2017 or after May 25, 2017.