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Evaluation, Screening and Diagnostic Testing for Determination of Clinical Trial Eligibility
International Research
Certificates of Confidentiality
External Adverse Event (AE) Reporting
eResearch Regulatory Management (eRRM)
Unanticipated Problems Involving Risks to Subjects or Others
Who May Consent for Participation in Research Studies (Michigan)
Investigator Responsibilities

Guidance

Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

International Research

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Certificates of Confidentiality

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

External Adverse Event (AE) Reporting

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

eResearch Regulatory Management (eRRM)

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Investigator Responsibilities

Updated on: