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34594 Conferences

How Accurate Adverse Event Reporting is the Key to Subject Safety of approved drugs

Added by Referral on 2010-07-15

Conference Dates:

Start Date Start Date: 2010-08-04
Last Date Last Day: 2010-08-04

Conference Contact Info:

Contact Person Contact Person: admin
Email Email:
Address Address: 2600 E. Bayshore Road, Palo Alto, CA, 94303, United States
Phone Tel: 650-620-3915
Phone Fax: 650-963-2556

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: rce/control/trainingFocus/~product_id=70 1634?channel=worldconf
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