This year’s event will look at innovative tools and methods for predicting site success, enhancing communication between all stakeholders, trial evaluation and termination, cultural considerations for site selection and highly-specified patient recruitment. Attendees will hear perspectives from industry, patients, investigators, study coordinators, and regulatory agencies and gain a better understanding of where the key challenges are and the emerging trends are to overcome them.
Why Attend? - Evaluate and better predict a site’s true recruitment potential through metrics and other tools.
- Enhance communication with sites to ensure engaged and motivated site staff
- Understand how cultural differences will affect patient recruitment potential and your study execution in emerging markets
- Learn how patient advocacy groups can be leveraged to enhance the outcome of a trial
- Improve cost efficiency by understanding where costs associated with clinical site selection go and how to manage these costs
Who will benefit?PHARMA: VPs, directors, managers of Clinical Research, Clinical Operations, Patient Recruitment, Clinical Quality Assurance, Medical and Regulatory Affairs, Medical Directors, Clinical Project Managers, Clinical Study Managers, CRAs.
CROs and SMOs: Business Development and Clinical Operations
CLINICAL SITE: Professors, Investigators, Study Nurses
For Booking Information contact:Erika Vavrovicova
Tel: +421 232 660 382
Fax: +421 2 3301 0331
Email:
[email protected] 
