This is the second Clinical Trials developed by the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy.
It is part of an engaging and interactive educational programme built to improve professional knowledge, skills and confidence of participants involved in clinical trial planning and design.
Highly interactive sessions are coordinated by top experts in their fields. In addition, courses offer interactive workshops on Good Clinical Practice (GCP), regulatory issues, statistics, trial data interpretation and manuscript writing.
29th May 2015 in NH Hotel Vittorio Venetto, Rome, Italy
Giuseppe MC Rosano, MD, PhD, FESC
Sven Wassmann, MD, PhD, FESC
An overview of the different aspects of clinical trials
Claudio Ceconi, FESC
Traditional vs novel trial designing
Giuseppe M.C. Rosano, MD, PhD
Clinical Trials: How to do them?
Basil S. Lewis, MD, FRCP, FACC, FESC
The team, the procedures, the monitor and the Sponsor
Lucy H H Parker, Clinical Research Governance Manager
Requirements from regulatory agencies: endpoints, comparators, type of studies
The Role of the Research Office
MaryCate MacLennan, R&D Performance & Delivery Manager
The Role of the PI: Keys to Success, Perils and Tribulations
Heinz Drexel, MD, FESC, FAHA
Good Clinical Practice (GCP) - A whistle stop tour!
Debbie Rolfe, Regulatory Assurance Manager, Joint Research & Enterprise Office
Controlled studies and registries
Christian Torp-Pedersen, Aalborg University
Meta-analysis and systematic review
Gianluigi Savarese, MD, FESC, ACC FIT
Post marketing surveillance
This initiative is supported in the form of an unrestricted educational grant from
Our mission: To reduce the burden of cardiovascular disease
© 2017 European Society of Cardiology. All rights reserved