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Clinical Compliance 2012 - Audit/Inspection Preparedness for Clinical Research/Site Coordinators

Date2012-03-06

Deadline2012-03-06

VenuePalo Alto, USA - United States USA - United States

KeywordsClinical Site Audit; Clinical Site Inspection; Audit preparedness; Inspection preparedness; regulatory requirements; sponsor requirements; guidelines; SOPs; ICH-GCP; FDA 21CFR312

Websitehttp://www.complianceonline.com/ecommerc...

Topics/Call fo Papers

This webinar on clinical site audit/ inspection will outline the responsibilities of the Investigator and the clinical research coordinator during and after site audits/inspections and show what you must do to ensure preparedness at all times.


Why Should You Attend:

The Clinical Research Coordinator (CRC) plays a key role in the site’s success at audits/inspections, and must therefore know how to ensure the site is ready for an audit or inspection at all times.

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Last modified: 2012-02-10 15:41:31