Production and Process Controls for Medical Device Companies

Posted By : User Ref No: WURUR56161 0
  • Image
  • TypeWebinar
  • Image
  • Location Fremont, California, United States
  • Price
  • Date 06-05-2020
Production and Process Controls for Medical Device Companies, Fremont, California, United States
Webinar Title
Production and Process Controls for Medical Device Companies
Event Type
Webinar
Webinar Date
06-05-2020
Last Date for Applying
05-05-2020
Location
Fremont, California, United States
Organize and Presented By
Compliance4all
Sponsored By
Compliance4all
Organizing/Related Departments
Online Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Business Development

Administration/Management

Manufacturing

Location
Fremont, California, United States

Overview:

Production and Process Controls (P&PC) are one of the key capabilities necessary for medical device companies to consistently and effectively produce safe and effective products.

Because Production and Process Controls are so critical they are one of the major subsystems emphasized in inspections by the FDA.

Why you should Attend: Failure to adequately implement Production and Process Controls (P&PC) can lead to disaster for your company or even worse for your customer. And P&PC continues to be a leading cause of 483 and warning letter observations from the FDA.

Even more alarming, P&PC failures are a leading cause for complaints, malfunctions, and product recalls. This webinar can help you prevent serious issues such as these.


Areas Covered in the Session:

  • Establishing P&PC
  • Change Control
  • Environmental Control
  • Personnel Requirements
  • Contamination Control
  • Buildings
  • Equipment
  • Manufacturing Material
  • Automated Processes
  • Inspection, Measuring, and Test Equipment
  • Process Validation
  • Linkages to the total product life cycle and risk management
  • Process Improvement


Learning Objectives:

  • Overview of the Regulations
  • FDA Expectations
  • Lessons Learned and Common Mistakes
  • Best Practices
  • Preparing for an FDA Inspection


Who Will Benefit:

  • Auditors
  • Quality Engineers
  • Manufacturing Engineers
  • Engineering Managers
  • Manufacturing Supervisors
  • Manufacturing/ Production /Operations Supervisors, Managers, and Directors
  • Plant Managers
  • Quality Managers
  • Employees new to Medical Device Companies

 

 

Speaker Profile

Susanne Manz ,MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. While at GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, WW Director of Quality Engineering and, Design Quality, and Director of Corporate Compliance. Susanne has a BS in Biomedical Engineering and an MBA from the University of NM.

Event link:

https://www.compliance4all.com/webinar/--502945LIVE?channel=eventsget-May_2020_SEO

Contact Info

Netzealous LLC, DBA -Compliance4all

Email: [email protected]

Phone: +1-800-447-9407

Website: https://www.compliance4all.com/

Others Details

Contact Info Netzealous LLC, DBA -Compliance4all Email: [email protected] Phone: +1-800-447-9407 Website: https://www.compliance4all.com/

Registration Fees
Available
Registration Fees Details
$150
Registration Ways
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Landmark
California
Official Email ID
Contact
Netzealous LLC,DBA -Compliance4all

39658 Mission Boulevard, Fremont, CA 94539, USA.

[email protected]

   8004479407    Fax No: 94539