Fundamentals of Toxicology - US edition MasterClass

This will allow non-toxicologists to learn the jargon and be able to effectively communicate with colleagues. In addition, the MasterClass will describe the basics of toxicology to allow non-specialists to understand the content of a toxicology report. 

09-12 May, 2023, Virtual

Time Zone: Eastern Standard Time (EST) / UTC−05:00

Overview

In toxicology, it should be possible to distinguish expected pharmacology (related to the mechanism of action of the drug) from unexpected or abnormal pharmacology. Toxicity should also allow to rank molecules based on their intrinsic toxic potential and to identify potential adverse effects. These effects should be correlated in toxicology with the exposure, to assess the presence of a dose-response. Overall toxicology studies should allow to extrapolate from non clinical data the human situation. This will allow the inclusion of suitable assessments during clinical development to ensure that safety of the enrolled subjects (either healthy volunteers or patients) is maintained. In addition, toxicology studies should allow the identification of patients at higher risk of an adverse event that should be excluded for the initial phases of drug development if this is deemed necessary. The MasterClass will cover these aspects that are relevant for non-toxicologists involved in drug development.

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RECOMMENDATION

Who should attend?

This course is aimed at anyone who encounters toxicology and safety data. The course is designed to give an overview of the field and it will be of particular benefit to professionals working in different departments including:

• Research & Development

• Preclinical Development

• Pharmaceutical Development

• Licensing & Business Development

• Clinical Operations

• Regulatory Affairs

• Clinical Pharmacology and Pharmacovigilance

• Medical writing

• Licensing

• Project Management

• Business Development