Αποτελέσματα Αναζήτησης
23 Μαρ 2023 · Use the most recent IRB sample forms. Current sample forms are available here. Don’t try to reinvent the wheel or assume that a previously approved form is the best template for all studies. Pay special attention to HIPAA Authorization language.
Use the categories and accordions below to identify the appropriate policy, procedure, or guidance needed. Then click the “Current IRB Policies and Procedures” button to open the searchable and hyperlinked PDF document to review the appropriate policy, procedure, or guidance.
This user-friendly application process has been streamlined to present users with only the questions relevant to their research. The new IRB ePortfolio utilizes branching logic with specific questions to better ascertain the regulatory information necessary to make IRB determinations.
5 Νοε 2012 · One of the IRB-approved forms used to document departmental review for scientific and scholarly merit; required for gene therapy and some other projects. Version: September 22, 2011
The UAB IRB requires Principal Investigators and all other research team members to complete and document appropriate training in the protection of human subjects. Additionally, the IRB monitors ongoing research for adherence to applicable regulations, policies, and procedures.
Several sections under General Information contain guidance about consent and assent: IRB-Review—Outcomes-and-Approval-Details; Conducting the Protocol; Participant Populations; The UAB IRB also offers a sample consent form written for a fictitious protocol. In most places, the sample demonstrates effective use of language at an 8th-grade ...
Several preliminary steps must be completed before the IRB can review any application. Completing these steps as described can help investigators avoid delays in receiving review by the IRB.
