Data Collection & Management in Clinical Trials 2010 November 23, 2010

The Data Collection and Management in Clinical Trials Asia 2010 is the first event exclusively focusing on patient compliance and data management strategies in Asia, an area of increasing popularity for building world-class data management centres. The event will gather key pharmaceutical companies, CROs, regulatory officials, as well as data capturing and management solution providers together under one roof. It will discuss opportunities and form strategic partnerships to leverage the enormous amount of opportunities the region has to offer.
Key themes for Data Collection and Management in Clinical Trials Asia 2010:
•What opportunities does Asia offer in managing global data for clinical trials; how should global pharmaceutical companies address the challenges and seize the opportunities from this increasingly important hub for clinical trials.
•How can pharmaceutical companies and sponsors stay abreast of clinical trial practices by improving efficiency and reducing cost in collecting and managing clinical data;
•How should CROs organize themselves to address sponsors’ requirements and play the role of a strategic partner in reducing trial time and complying with regulatory requirements;
•What regulatory considerations should the industry bear in mind in the process of data collection, transmission and in regards to data security;
•What are the software and hardware developments to date, and how should pharmaceutical and CRO companies leverage such development to improve the efficiency of data collection and management for clinical trials

Official Website: http://www.clinical-trial-data.com/