Online Event on HazardAnalysis 2014 - How to Conduct a Hazard Analysis/Risk Assessment
Date2014-07-22
Deadline2014-07-22
VenueOnline Event, USA - United States
KeywordsCompliance Training; Regulatory Training; Pharma; Clinical; Health
Websitehttps://bit.ly/1kgSsEn
Topics/Call fo Papers
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
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - bit.ly/1kgSsEn
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
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - bit.ly/1kgSsEn
Other CFPs
- Update on FDA 510(k) Review Process, Hurdles and Good Practices on 510(k) Preparation and Clearance
- ISO 13485: 2003 - A Straightforward Interpretation with Recommendations for Easy Implementation
- Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
- HACCP Validation and Verification
- Understanding and Preparing for FDA's on-going Part 11 Inspection Program
Last modified: 2014-06-06 13:58:09