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Event Details
Learn how to perform risk assessment as part of the risk-based approach to computer system validation.
Why Should You Attend:
This webinar will show how you can determine and document risk in a process to reduce system validation time and ensure compliance.
The presenter will share real life examples that make application of the techniques, covered in this webinar, understandable in the context of any validation project. The training will include a workshop for participants to perform their own hazard analysis so they are proficient in applying the risk-based techniques.
Areas Covered in the Seminar:
- How to identify risk and plan risk-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:
This course benefits anyone that uses computer systems to perform their job functions and is ideal for regulatory, clinical, laboratory, and IT professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors.
- IT/ IS
- QA
- QC
- Laboratory staff
- Managers
- GMP, GCP, GLP professionals
For Registration :
http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=700896?channel=Eventbrite
When & Where
Online Webinar
2600 E. Bayshore Road
Palo Alto,
CA 94303
Tuesday, September 18, 2012 from 10:00 AM to 11:00 AM (PDT)
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