When: |
16 Mar through 16 Mar 2017 | |
CFP Deadline: |
16 |
|
Where: |
Online Event | United States | |
Website URL: |
http://www.compliance4all.com/control/w_product/~product_id=501190LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Mar_2017_SEO | |
Sponsoring organization: |
Compliance4All | |
Categories: |
Education / Legal / Other - Other |
Keywords:
Event description:
Overview:
Risk Assessment is a fundamental expectation in the regulated industries of pharmaceutical and medical devices. Performing risk assessments can be interpretive and needs to be well thought out in order to rationalize and substantiate conclusions drawn.
Why should you Attend:
The reason for attending would be to gain a perspective and understanding of the proper application of risk assessment. The proper practice of Risk Assessment is the current expectation of regulatory authorities.
Areas Covered in the Session:
The regulatory derivations of Risk Assessment
The expectations of risk
How to properly analyze and determine risk
The fundamental equations necessary for risk assessment
The tools of Risk Assessment and their definitions
How to defend and assign proper risk
Who Will Benefit:
QA specialist
Managers
Engineers
Operators
Speaker Profile:
Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of ex...
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Posting date:
11 January 2017 | 171 views
Placement:
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