Informed Consent - Module 4s Sec 0


Module 4 Objectives
Continuing Review
Unanticipated Developments
Adverse Events
Consent Document Revisions

Module 4 Objectives

fter completion of this module, you should be able to:
  • describe the frequency of continuing review,
  • determine the review outcome of unanticipated developments,
  • determine the review outcome of adverse events, and
  • list the criteria for consent document revision.
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