pharmaceutical 2017 - Understanding Proper Application of Risk Assessment

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 experience in Quality Assurance, Quality
Control, Validation, consent decree remediation as well as cGMP
Compliance in the Medical Device and Pharmaceutical industries. Lou has
worked for several well know companies inclusive of Johnson & Johnson,
Bristol-Meyer Squibb, Pfizer, Schering Plough and Merck.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com