ComplianceOnline

Supplier Quality Agreements - Essential for Suppliers of Many Outsourced Processes

Instructor: Betty Lane
Product ID: 703515
  • 29
  • March 2017
    Wednesday
  • 10:00 AM PDT | 01:00 PM EDT
    Duration: 60 Min

Live Online Training
March 29, Wednesday 10:00 AM PDT | 01:00 PM EDT | Duration: 60 Min

$199.00
One Dial-in One Attendee
$399.00
Group-Max. 10 Attendees/Location
(For multiple locations contact Customer Care)

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section 48 hrs after completion of Live training

Training CD

$349.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days after completion of Live training

Combo Offers

Live + Recorded Version

$349.00

Live + Training CD

$399.00

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar will discuss in detail the use of the Global Harmonization Task Forces (GHTF) and Notified Body Operations Group (NBOG) supplier guidance documents to create QA agreements. Attendees will learn best practices to ensure compliance with FDA and EU guidelines for supplier quality agreements.

Why Should You Attend:

Detailed supplier Quality Assurance (QA) agreements with key suppliers whether standalone or part of a larger supplier agreement are becoming essential as more medical device companies are looking to increase their outsourcing. Both ISO 13485 European Notified Bodies and the FDA are requiring companies to create detailed agreements with their key suppliers. The 2008 GHTF supplier guidance document is now an expectation of both the FDA and most ISO 13485 auditors. These auditors must verify that you have objective evidence of control of product and service suppliers. Supplier QA agreements can be an important part of demonstrating this control. In addition, the operations group for European Notified Bodies (NBOG) released a guidance document in 2010 outlining how your ISO 13485 auditors should audit you.

This webinar will provide an understanding of what the current guidance documents suggest be included in supplier agreements. In addition to defining the content of a supplier agreement, this presentation will help you decide who needs these agreements and how best to implement them. Supplier control has always been an FDA and ISO 13485 requirement, but the current expectation is that you actually document how you are doing this control as part of your supplier management program. QA agreements can be an easy way to demonstrate this control for key or critical suppliers. This presentation will help you prepare for the current expectations of FDA and ISO 13485 notified bodies by demonstrating that you have sufficient control of your key suppliers.

Learning Objectives:

  • To learn why QA agreements are necessary and desirable
  • To review which suppliers need QA agreements
  • To understand contents of supplier QA agreements

Areas Covered in the Webinar:

  • Types of suppliers that should have QA agreements to ensure FDA and ISO 13485 compliance
  • Explanation and use of the Global Harmonization Task Forces (GHTF) and NBOG supplier guidance documents to create QA agreements
  • How to create supplier QA agreements and the best way to implement them
  • Definition of and requirements for critical suppliers
  • Supplier agreements best practices

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

  • Quality Management
  • Regulatory Affairs
  • Supply-chain Management
  • Supplier Engineering
  • Purchasing Management
  • Supplier Auditing
  • Internal Auditing
  • Consultants to Medical Device Companies
Instructor Profile:
Betty Lane

Betty Lane
Founder and President, Be Quality Associates LLC

Betty Lane, has over 30 years’ experience in medical device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems for both FDA and ISO 13485 compliance band business when they became FDA and industry requirements. Her are areas of expertise include training, auditing, supplier management, design controls, software validation and general safety.

Betty’s training experience includes over 25 years of training on all areas ISO 13485 and FDA cGMP, in companies where she worked as manager or director, and for AAMI, ASQ biomedical division, and ASQ sections. She has taught courses in medical quality and regulatory affairs as an Adjunct at Northeastern University, Boston, MA. Betty is active in her local section of the American Society for Quality and is also a member of the RAPS, Association for the Advancement of Medical Instrumentation (AAMI), The Society of Women Engineers and the IEEE. Betty has degrees in engineering from Rensselaer Polytechnic Institute, and an MBA from Northeastern University.

Topic Background:

Quality Assurance (QA) agreements are usually more flexible than standard supplier agreements and can therefore be more detailed and easier to modify than standard supplier contracts which often require legal as well as management approval. QA agreements with your suppliers can be the easiest way to assure both your company and auditors that you have sufficient control of your key and critical suppliers. QA agreements give details of who is responsible for what between you and your supplier. Yet, because these agreements are detailed and specific to a particular supplier, they should only be used for those suppliers where they provide value. Even if your key suppliers are only from different branches of your own company, a supplier QA agreement can be an important tool to show the FDA and ISO 13485 Notified Body auditors that you have the required control of these suppliers.

Follow us :
ComplianceOnline Banking Summit 2016 | Risk Management and Data Security - 80390SEM
ComplianceOnline Medical Device Summit 2017

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed
    Loading