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.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:
Quality Management
Regulatory Affairs
Supply-chain Management
Supplier Engineering
Instructor Profile:
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.
Note:
Use coupon code 232082 and get 10% off on registration.
For Registration:
http://www.complianceonline.com/fda-supplier-quality-agreements-for-outsourced-processes-webinar-training-703515-prdw?channel=sciencedz