This drug safety training will discuss the various factors to be considered and the principles of risk assessment to be followed during drug development to minimize risk.
Areas Covered in the Seminar:
Risk conceptualization.
Goals of project risk management.
Risk management planning & safety review teams.
Intellectual property.
Pharmacovigilance planning in product risk management.
Unexpected study results: efficacy, dosage, adverse events & toxicology.
Data analysis, interpretation and presentation.
Essentials of Data Monitoring Committees.
Drug disposal and environmental impact.
Labeling as a hallmark of risk management efforts.
Post-marketing risk.
Past Events
Drug Safety Assessment and Risk Minimization in the Development Period 2010 - 26 Oct 2010, Webinar (9428)
Important
Please, check "Drug Safety Assessment and Risk Minimization in the Development Period" official website for possible changes, before making any traveling arrangements
