Applying Principles of 21 CFR Part 820 Quality System Regulation

7 years ago Posted By : User Ref No: WURUR10725 0
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  • TypeWebinar
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  • Location San Diego, California, United States
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  • Date 14-03-2017
Applying Principles of 21 CFR Part 820 Quality System Regulation, San Diego, California, United States
Webinar Title
Applying Principles of 21 CFR Part 820 Quality System Regulation
Event Type
Webinar
Webinar Date
14-03-2017
Last Date for Applying
13-03-2017
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:  
In this webinar, we apply the Theory of Lean documents and its corollary Theory of Lean Configuration to present a fresh approach to following 21 CFR Part 820. 

Product Id : 501083

Instructor : Jose Mora

Tuesday, March 14, 2017   |   10:00 AM PST | 01:00 PM EST   |   Duration: 60 Minutes

WHY SHOULD YOU ATTEND:
If you are constantly struggling to create, manage, and maintain all of the information found in controlled documents, all of which are often redundant, repetitive, and clustered together in an awkward manner, this webinar is something that will give you a different perspective and a very different approach that you can use.

AREAS COVERED IN THE SESSION:

  • Brief introduction to Lean Documents and Lean Configuration
  • Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to design control documents
  • Basic functions found in a life sciences manufacturing plant
  • Key types of controlled documents and records for manufacturing
  • Quality Management System (QMS) elements controlled via documentation
  • Bringing it all together

WHO WILL BENEFIT:

  • Managers, Supervisors, Directors, and Vice-Presidents
  • R&D
  • Manufacturing Engineering
  • Design Assurance
  • Quality Assurance
  • Operations
  • Document Control

SPEAKER PROFILE:
Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

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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]

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   Fax No: 302-288-6884