Understanding Risk Assessment of Proper Application

8 years ago Posted By : User Ref No: WURUR10728 0
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  • TypeWebinar
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  • Location San Diego, California, United States
  • Price
  • Date 16-03-2017
Understanding Risk Assessment of Proper Application, San Diego, California, United States
Webinar Title
Understanding Risk Assessment of Proper Application
Event Type
Webinar
Webinar Date
16-03-2017
Last Date for Applying
15-03-2017
Location
San Diego, California, United States
Organization Name / Organize By
Compliance4All
Organizing/Related Departments
Healthcare Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Accounting/Financial/Banking/Insurance

Medical/Healthcare/Hospital

Location
San Diego, California, United States

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:

  • 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.

Others Details

For more details and updates please visit webinar website

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: US$150.00
Registration Ways
Email
Phone
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Official Email ID
Contact
Event Manager

Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: [email protected]

[email protected]

     +1-800-447-9407
   Fax No: 302-288-6884