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.

International Institute of Medicine & Science, Inc.