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Death By CAPA - Does your CAPA Program Need a CAPA?

Event Details

Death By CAPA - Does your CAPA Program Need a CAPA?

Time: February 25, 2020 from 10am to 1pm
Location: Online
Street: 39658 Mission Boulevard, Fremont, CA 94539, USA.
City/Town: United States
Website or Map: https://www.compliance4all.co…
Phone: +1-800-447-9407
Event Type: online, event
Organized By: Compliance4all
Latest Activity: Dec 10, 2019

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Event Description

This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company.

You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

We'll discuss best practices so you can start off on the right foot and always be prepared for an inspection.

Why you should Attend:CAPA is the corner stone of an effective Quality Management System. Yet, it frequently perceived as a burdensome and bureaucratic exercise. Many companies struggle to establish and maintain a CAPA program that is efficient and effective. An ineffective CAPA System leads to disastrous consequences such as medical device reports, recalls, 483s, and warning letters. And an inefficient CAPA program results in wasted time, money, and missed opportunities. In this webinar, we'll discuss the fundamentals of a CAPA program and how you can make your CAPA program more efficient and more effective.

Areas Covered in the Session:

  • FDA and NB expectations for CAPA
  • Lessons Learned from 483s and warning letters
  • Common problems and simple solutions
  • How to structure your CAPA process
  • How to use IT tools to monitor and maintain your CAPAs
  • Metrics to ensure your CAPAs are timely and effective
  • A toolkit for CAPA

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

Who Will Benefit:
  • Quality Systems Specialists
  • Document Control Specialists
  • Quality and Compliance Specialists
  • Internal Auditors and Managers
  • Training Specialists
  • CAPA Specialists
  • Supplier Quality Engineers and Auditors
  • Quality/Compliance Managers or Directors for Medical Device companies
  • General Managers wanting to learn how to understand Quality System Requirements

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/--502862LIVE?channel=%20medtechiq.ning_2020_SEO

Contact Info

Netzealous LLC,DBA -Compliance4all

Email: support@compliance4All.com

Phone: +1-800-447-9407

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

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