Course Overview

Adverse Drug Reactions (ADRs) are a major clinical problem. An understanding of the clinical aspects of ADRs is a fundamental requirement for any professional in the field of pharmacovigilance. The Medical Aspects of Adverse Drug Reactions course provides delegates with the opportunity to acquire concentrated instruction on the strategy of therapeutics, medical diagnosis and all medical aspects of ADRs. It is divided into individual body systems (such as hepatic, endocrine, haematological, neurological, psychiatric, cardiovascular, oncological, gastrointestinal, renal and respiratory) and general concepts of ADRs.

*Please note that the course dates and programme may be subject to change.

This course is aimed at:

• Pharmaceutical industry personnel from areas including pharmacovigilance, clinical research, medical affairs,medical writing, regulatory affairs and medical information
• Staff from regulatory authorities
• Clinicians and academic staff
• Pharmacists or other professions allied to medicines