Course participants will come away with practical knowledge to improve their understanding of the breadth of this fascinating subject. Discussed will be the role of toxicology in all stages of drug development, the regulatory environment under which toxicologists work, and interpretation of tox data. Practical exercises and discussion sessions cover case studies for a wide variety of drugs and indications. Acceptable safety margins for different therapeutic areas, and how these affect the interpretation of toxicology data is also examined. Improve your confidence when interacting with toxicologists on your project team.

Who Will Attend?
This course is designed for all those who come into contact with toxicology data, but who are not specialist toxicologists. Participants may be from preclinical and clinical development, regulatory affairs, project management, drug safety, registration and data management. No previous knowledge of toxicology is assumed.

Course Leader
The course will be led by 2 experienced toxicologists who each have nearly 20 years extensive knowledge of preclinical development both from a pharmaceutical company and contract organisation perspective. Both course leaders are well published in all aspects of toxicology and speak regularly on the subject.

Registration required:

Yes

Free:

No