Date :
Place : United States, Fremont
Website :http://www.compliance4all.com/control/w_product/~product_id=500480LIVE/
Contact Person:Adam Fleaming
Description:
The proper practice of Risk Assessment is the current expectation of regulatory authorities. Many regulatory related documents and guidance now speak of the application of risk throughout a process inclusive of qualification and validation.Deadline for abstracts/proposals : 14th September 2015
Organized By :Compliance4All
Keynote Speakers : 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. This work experience was acquired either as a direct employee or as a contracting consult
Conference Highlights :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
Venue :online event
Check the event website for more details.