Applying for IRB Review
Whether you are a seasoned or novice investigator interested in conducting
research at CVMC, the resources needed for developing your proposal for
IRB review can be found here. Protecting Human Research Participants (PHRP)
training is required for the primary investigator, co-investigator(s),
and key study personnel prior to submitting an IRB application. If requesting
review of a FDA-approved clinical trial, Good Clinical Practice (GCP)
training is required. The
Roche TransCelerate-approved GCP course is online and free of charge.
To access the Investigator Manual, IRB Application, Submission Cover Memo,
Informed Consent Checklist, Consent Waivers Request, Continuing Review
& Closure Form, etc., click on the following links. Consult Kimberly
Yates, Department for Research and Evidence-Based Practice Administrator,
prior to beginning the research process at
research@cvmc.us or 828.326.3251.
Investigator Manual
IRB Application Submission Cover Memo
Informed Consent Checklist
Informed Consent or Assent Waiver Request
Student Project Request
Continuing Review & Study Closure Form