Conference Description:
In this Clinical compliance training learn how to assess record and manage the adverse events occurring during conduct of clinical research utilizing human subjects and how to avoid the common mistakes.
Areas Covered in the Seminar :
The CFR definitions of Adverse Events, Serious Adverse Events, Unanticipated Adverse Device Effects and many more.
How to know what an Adverse Event is and when to report it or them.
Understanding laboratory AEs and the "Reference Range" concept.
Common Mistakes in AE / SAE Reporting.
Reporting of Adverse Events - when and to whom and the use of AE Terminology systems
The Role of Data safety Monitoring in Protecting Human Volunteers
How to record Adverse Events and assess causality - the algorithm
For More Details:
http://www.complianceonline.com/ecomme rce/control/trainingFocus/~product_id=70 1634?channel=worldconf
Start Date: 2010-08-04
Last Day: 2010-08-04
Contact Person: admin
Email: admin@complianceonline.com
Address:
2600 E. Bayshore Road, Palo Alto, CA, 94303, United States
Tel: 650-620-3915
Fax: 650-963-2556
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