Policies and Guidances Relating to Monitoring

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Home > Monitoring > Policies and Guidances Relating to Monitoring

Guidances & Policies

Guidances

How and When a Principal Investigator Should Report Death of a JHM Research Participant

Humanitarian Use Devices (HUD)

I. Informed Consent Guidance

II. Informed Consent Guidance - How to Prepare a Readable Consent Form

III. Informed Consent Guidance - FDA Regulated Studies

Investigational Medical Devices

Investigators as Study Participants (Self-Experimentation)

Reporting Protocol Deviations

Research Using FDA Test Articles

Policies

Organization Policy on Reports of Unanticipated Problems Involving Risks to Participants or Others (Policy No. 103.6(b))

Organization Policy on Investigator Non-Compliance (Policy No. 103.7)

Organization Policy on Complaints from Research Participants, Investigators and Research Staff, the Community, etc. (Policy No. 109.3)

Organization Policy on Monitoring the Consent Process and Research Procedures in Ongoing Research (Policy No. 109.8)

If you have any comments, questions or suggestions
you may contact the JHM IRB at:

p: 410.955.3008 | f: 410.955.4367 or 443.287.5353 | e: jhmirb@jhmi.edu