Scheduling Activities through Qualtricsįor studies that involve accessing FERPA records for research purposes, there are some required letters that need to be submitted with the IRB application.Optional Interview/Focus Group/Lab Visit Confirmation and Reminder Emails.Optional Interview/Focus Group/Lab Visit Scheduling.Researchers can take these templates, edit them to match their study procedures, and then submit the clean and edited documents to the IRB with their study application. These are templates for communicating with participants about activities occurring in the study. The NC State IRB has some optional templates that researchers can use when designing their study. View form Communication with Participants The minor assent form templates have stock language discussing broad consent for minors aged 11 and up that a research team can use if appropriate, but it must be used in conjunction with seeking parent/guardian permission for broad consent. There are two templates: one for adult participants and one for parents/guardians of a minor participant.However, the use of this identifiable/re-identifiable data where Broad Consent was obtained may undergo Administrative review resulting in Exemption, where without Broad Consent, the use of the identifiable/re-identifiable data would require mid-level (Expedited) review and approval. When the researcher wants to use the identifiable/re-identifiable data for which Broad Consent was sought and obtained, they are required to apply for IRB approval through NC State.If a researcher sought Broad Consent from participants in an IRB-approved study, the researcher must track which participants did and did not say yes to Broad Consent.Broad consent can never be required of participants and carries some additional researcher responsibilities.Unspecified research is where the participant is not informed of the nature of the research or the purpose of the research.Report Unanticipated or Adverse Events Formīroad consent allows the researcher to keep a participant’s re-identifiable or identifiable information or biospecimens for future unspecified research if the participant (or parent/guardian and child, if researching minors) agrees.Veterinary Verification and Consultation (VVC) Reviews.Use of Restraint in Vertebrate Animal Studies.Use of Non-pharmaceutical-grade Compounds in Live Vertebrate Animals.Tracking of Approval and Approved Animal Numbers.Review Procedures for Significant Changes in an Approved Protocol.Required Health/Medical Record Keeping for Research and Teaching Animals.Procedure for Semiannual Facility Inspections.Needs for Prospective Clinical Studies Using Client-Owned Animals.Guidance on Activities Requiring IACUC Approval.Disposition of Research and Teaching Animals. Classification of Animal Use by Pain and Distress Categories.Conducting Research Outside the United States.
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