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All About Clinical Trials - May 2015 - Rome - IT

The Educational Programme of the ESC Working Group on Cardiovascular Pharmacotherapy

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.

2nd Course: All About Clinical Trials

29th May 2015 in NH Hotel Vittorio Venetto, Rome, Italy 

Course directors

Giuseppe MC Rosano, MD, PhD, FESC

Sven Wassmann, MD, PhD, FESC

Sessions and resources

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

Giuseppe M.C. Rosano, MD, PhD

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

Claudio Ceconi