International Institute of Medicine and Science, Inc.

PROGRAMS - EDUCATION

Scientific Research Methodology

Part 1: The Scientific Method.
Part 2: Medical and Methodological Standards.

Part 3: Probabilistic Measures of Diagnostic Tests.

Drug Development Trials

Part 1: Regulatory Requirements.

Part 2: The Drug Delivery Process.

Part 3: Trial Phases.

Clinical Trials - Investigators' Responsibilities

Part 1: Summary of Regulatory Responsibilities.
Part 2: Form FDA 1572 para 9 ("Statement by Investigator").
Part 3: ICH GCP and FR Guideline.

Investigators' Responsibilities for Records

Part 1: Study Binder.
Part 2: Source Documents.
Part 3: Standard Operating Procedures (SOPs).

Investigators' Financial Disclosure Responsibilities

Part 1: Definitions.

Part 2: Financial Arrangements.
Part 3: Scope.

Part 4: Record Keeping and Retention.

Institutional Review Boards (IRB)'s Responsibilities

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