Drug Safety and Clinical Trials - A Concise Workshop

Contenido de curso
This foundational one day course on the essential aspects of clinical safety is designed for everyone involved in clinical research activities.

This course provides key definitions based on the new European Community legislation as well as on consensus forums such as ICH and the CIOMS Working Groups. Practical examples and workshops are intended to illustrate these definitions and introduce the skills needed to perform clinical safety tasks successfully.

Objetivos de formación
Identify key definitions and vocabulary used in clinical safety in the EU. Recognise important aspects in evaluating adverse events. Identify main characteristics of adverse events, etc.

Destinatario
Project Managers, CRAs & CTAs responsible for clinical operations, drug safety personnel, investigators, representatives of organisations including academia running clinical trials and medical managers from the pharmaceutical industry.

Oportunidad de trabajos y los campos profesionales mas buscados por personas ya tituladas
CRA, Clinical Research Associate, PM, Project Manager, Regulatory, Pharmacovigilance

Certificación
ISO9001:2008

Organizador local
ECCRT

Ms. Sunita Kelecom