This course provides the learner with a working knowledge of informed consent regulations, Institutional Review Board / Independent Ethics Committee responsibilities, and the obligations of the individuals responsible for protecting patient rights and welfare.

Topics include:
      ·          Protecting subjects
      ·          Consent forms
      ·          Consent process
      ·          Consent exceptions
      ·          IRB/IEC
      ·          Responsibilities
      ·          Procedures and records     

Linda Belmont at DIA