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Institutional Review Board submission service

eagle-i ID


Resource Type

  1. Support service


  1. Fee for service
  2. Resource Description
    The CRSO staff assists investigators who are preparing the following study documents for submission to the Institutional Review Board: • Initial submission • Informed consent documents • Continuing reviews • Study completion requests • External/internal serious adverse events • Safety reports • Protocol modifications and amendments • Protocol deviations • Recruitment materials and advertising • Consent form translations
  3. Topic
    Homo sapiens
  4. Service Provided by
    Clinical Research Support Office (CHOP)
  5. Website(s)
  6. Related Technique
    Human subject recruitment and protection
  7. Related Technique
    Clinical trial technique
Provenance Metadata About This Resource Record
Copyright © 2016 by the President and Fellows of Harvard College
The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016