Fundamentals of Toxicology MasterClass - EU edition

26-29 August, 2024

The MasterClass will cover aspects that are relevant for non-toxicologists involved in drug development

This masterclass 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.

26-29 August, 2024, Virtual
Time Zone: UTC/GMT+1 /CET

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Key learnings

Understanding

An understanding of the principles of practical toxicology

Deeper Insight

A deeper insight into the role of toxicology in the different phases of drug development

Strategies

Strategies to interact with a different company departments as far as toxicology is concerned

Explanation

An explanation of the principles of regulatory toxicology

Insight

An insight of the toxicology terminology

Description

A description of the concept of “safety margins”

Trusted by over 17,000 delegates across leading companies

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Pharma Online MasterClass

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 ranking of molecules based on their intrinsic toxic potential and to identification of 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 us to extrapolate from nonclinical data the human situation. This will allow the inclusion of suitable assessments during clinical development to ensure that the 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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Trainer

Dr. Stefano Persiani

Dr. Stefano Persiani is currently Director of Translational Sciences and Pharmacokinetics at Rottapharm Biotech, Italy. He graduated in Pharmacy at the University of Milan, Italy and completed a post-doctoral fellowship in the Department of Pathology of the University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania, USA, and later as a Research Associate in the Department of Pharmaceutics of the University of Southern California, School of Pharmacy in Los Angeles, California, USA. After these academic positions, he entered the pharmaceutical industry at Farmitalia Carlo Erba, Pharmacia, Upjohn, and Zambon Group and in the CRO sector with different managerial roles in drug R&D. Dr. Persiani is currently applying translational approaches from drug discovery to development and registration in several therapeutic
areas. He is a member of various international scientific societies and serves on the review board of numerous professional journals. Dr. Persiani acts as an external expert evaluator for the European Commission on the 7th Framework Program, Maria Sklodowska-Curie Individual Fellowships, HORIZON 2020, and Innovative Medicine Initiative, and for several other government organizations where he evaluates and provides recommendations on applications requesting funding. Dr. Persiani has many years of consulting, teaching and training experience in several fields of Translational Sciences.

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Reasons to attend a masterclass

Practical knowledge

Venture into undiscovered territories and gain inspiration through collaboration

Interactivity

Boost your professional skills by directly engaging with domain experts

World-class trainers

Gain value and learn from the best instructors

Networking

Build a top-notch community and advance your career

Who should attend img 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

Ticket options for you

Full event
pass

Team participation?

*minimum of 10 participants

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Testimonial

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey

Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi

USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej

Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany

About GLC

Global Leadership Conferences began as an ambitious dream by three founders ten years ago. Today it’s an international series of interactive events, exploring the hottest topics in critical fields. Each year, thousands of professionals join us to challenge the status quo and learn innovative ways to create new solutions in Finance, Pharmaceutical, HR, Health & Safety, and Energy.

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