How do I submit a Protocol for Continuing Review?

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Please submit all protocols to the Office of Research Compliance located in CBH Suite 160 during business hours (8 am – 5 pm).

Expedited Review:

Note that investigators must submit the appropriate amount of hard-copies for proper IRB review. No E-versions of research-related documents will be accepted.

(1) THREE (3) hard-copies of the following documents:

  • Progress Report Form (with original SIGNED copy)
  • Protocol Synopsis (current IRB-stamped version)
  • EACH CONSENT FORM (current IRB-stamped version)
  • Other IRB approved research-related documents (i.e. flyers, questionnaires, etc.)

(2) One (1) hard-copy of the following documents:

 

Full Board:

Note that investigators must submit the appropriate amount of hard-copies for proper IRB review. No E-versions of research-related documents will be accepted.

(1) Original SIGNED Progress Report with a CLEAN (hard) copy of EACH Consent Form

(2) Six (6) compiled packets containing the following documents (please collate documents):

  • Protocol Synopsis (current IRB-stamped version)
  • Informed Consent (current IRB-stamped version)
  • Recruitment ads, flyers, questionnaires, etc. (current IRB-stamped version)
  • Executive summary cover letter of any data safety committee or multi-center trial reports (if available/applicable)

(3) One (1) hard-copy of the following documents: