- TypeWebinar
- Location San Diego, California, United States
- Date 16-03-2017
Education/Teaching/Training/Development
Accounting/Financial/Banking/Insurance
Medical/Healthcare/Hospital
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.
Product Id : 501190
Instructor : Louis Angelucci
Thursday, March 16, 2017 | 10:00 AM PST | 01:00 PM EST | Duration: 60 Minutes
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:
WHO WILL BENEFIT:
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.
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Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: [email protected]
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