Live Webinar FDA Focus:Purchasing / Supplier Controls for Medical Devices
01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 90 Minutes
Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar
"Hear By Susanne Manz who holds Regulatory Affairs Certification (RAC) from RAPS and is a Certified Quality Auditor by the American Society for Quality."
Purchasing Controls have received significant scrutiny from the FDA in recent years due to an increase in adverse events and recalls.
This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn how to prevent quality and compliance problems by having a strong system for Purchasing Controls! This webinar will help you to understand the regulations and how you can translate them into an efficient and effective process for purchasing/ supplier control. You’ll learn about the essential elements of purchasing control and how you can translate them into your procedures. We’ll discuss the process steps for purchasing control and how it relates to other parts of your QMS including receiving and acceptance activities.
Why Should You Attend
Inadequate supplier/purchasing control can lead to a multitude of problems including rejections or delays at receiving inspection; non-conformances and scrap on your manufacturing lines; and quality problems that can manifest later in the field resulting in MDRs and recalls.
Purchasing Controls have received significant scrutiny from the FDA in recent years due to an increase in adverse events and recalls. Purchasing Controls continue to be a leading source of 483 and Warning Letter citations.
This 90-minute webinar will focus on establishing an effective and efficient system of purchasing controls. Topics to be covered include:
Understanding the regulations
Purchasing Controls Process
Evaluation of Suppliers
Feedback and Communication
Who will Benefit
Industries who can attend
This 90-minute online course is intended for professionals in the in electronics, automotive, retail, and medical device Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel