How to Conduct a Hazard Analysis/Risk Assessment - Webinar by GlobalCompliancePanel

Date	Feb 12, 2014
Time	01:00 PM EDT
Cost	$225.00
Online

Overview: This interactive webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance. 

What makes this session unique are the real life examples that make application of the techniques understandable in the context of any validation project. It includes a workshop for participants to perform their own hazard analysis so they are proficient in apply the risk-based techniques.

Areas Covered in the Session:

• Interactive real life examples.
• How to identify risk and establish mitigations.
• How to use the hazard analysis to make validation efficient. 
• How to document the risk assessment using a template
• How risk assessment reduces validation time.
• Determine risk in a process to reduce the testing effort. 
• Traceability made automatic
• Workshop exercises.

Who Will Benefit:

• All system users
• IT
• QA
• QC
• Laboratory staff
• Managers
• Executives

David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. He specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management. He has completed more than 185 mission critical software validation projects.

Contact Information:
NetZealous LLC,
DBA GlobalCompliancePanel 
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA          
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com    
http://www.globalcompliancepanel.com