Part 1. General concept of preclinical studies and their place in drug development. Definitions.
Part 2. Classification of preclinical studies and objects of study. Fundamental, translational and regulatory research.
Part 3. Analysis of requirements for the main types of safety studies.
Part 4. Standard Scope and Examples: Small Molecular Compounds, Biotechnological Products, Anticancer Drugs, Vaccines, Gene/Cell Therapy.