Overall Residual Risk Evaluation - Webinar By GlobalCompliancePanel

Website https://www.globalcompliancepanel.com/control/w_product/~product_id=600422?channel=mailer&camp=webin | Edit Freely

Category Health Care, Medical Device, Compliance Training

Deadline: April 20, 2011 | Date: April 20, 2011

Venue/Country: Wilmington, U.S.A

Updated: 2011-03-29 18:58:04 (GMT+9)

Call For Papers - CFP

Why you should attend: One of the most important Risk Management activities is the Overall Residual Risk Evaluation which occurs at the end of the development cycle to assure the product risk meets the risk acceptability criteria prior to issuing the Risk Management Report and release of the product. Companies have not had methods in place to perform this activity, and although some information appears in ISO 14971, there is not sufficient guidance on how to perform Overall Residual Risk Evaluation.

Areas Covered in the Session:

* Choosing the Evaluation Team

* Determining the Evaluation Process

* What documents should be part of the review?

* Using the Risk Chart in the review

* How to compare to the Risk Acceptability Criteria

* Documenting the results of the Evaluation

Who will benefit:

* Risk Managers

* Project Managers

* Quality Engineers

* Regulatory Managers

* Clinical Managers

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00