Webinar - Management & Integration of Non CRF Data

Course overview
This workshop aims to make Data Managers aware of the technical, clinical and regulatory considerations for non-CRF data handling. The principles covered in this course can be applied to any non-CRF data.

Who should attend?
This course is for Clinical Data Management and other professionals involved in any way with the handling of non-CRF data.

Content

• Types of data
• Standards
• Regulatory considerations
• Tools
• Data quality
• Vendor management

By the end of this course you will:
• Be able to identify the key considerations for non-CRF data collection
• Know how to effectively manage and integrate such data
• Have insight in to possible complications
• Know how to resolve issues
• Be able to identify what to communicate, to whom and how often

Course format
This 1.5 hour Webinar briefly covers all the key areas of non-CRF data handling within a clinical trials context. The session is highly interactive and participants will be encouraged to contribute to discussions and share their experiences.
 

This course will be held as a 'webinar' from 12:00 - 13:30 on Tuesday 12th January 2010.

Webinar participation is £300 plus VAT per location. There is no limit to the number of delegates participating from one location. However, all delegates must be in the same room and be sharing one telephone line to dial in. Proceeding to book a place on this course you are agreeing to our terms and conditions.

Click here to view the terms and conditions.