| |
|
|
|
ComplianceOnline, Online Event
2012-09-25
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.
Event Details: Date: September 25, 2012 Time: 10:00 AM-11:00 AM PDT Cost: $249 per attendee per computer terminal Registration: SIgn-Up on-line now. Add to your shopping cart. |
|
|
|
|
|
|
|
Organized by:
|
|
ComplianceOnline |
|
|
Invited Speakers:
|
|
David Nettleton , Computer System Validation's principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, software validation, and computer system validation. He is involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications.
|
|
|
|
|
|
|
|
Deadline for Abstracts:
|
|
2012-09-25
|
|
|
|
|
|
|
|
Registration:
|
|
http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=700896?channel=hummolgen
|
|
|
E-mail:
|
|
referral@complianceonline.com
|
|
|
|
|
|
|
|
|