Date :
Place : United States, Seattle
Contact Person:John Robinson
Description:
This seminar will go into the details of the NBOG supplier guidance document and a GHTF (Global Harmonization Task Force) guidance that describes the current FDA expectation on supplier management.Deadline for abstracts/proposals : 31st January 2017
Organized By :NetZealous DBA GlobalCompliancePanel
Keynote Speakers : 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. Her work enables companies to manage their business in compliance with FDA and ISO 13485 requirements, as well for quality syst
Conference Highlights :Overview: Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. Why should you attend: Since FDA regulat
Venue :Courtyard Seattle Sea-Tac Area, West Valley Highway, Tukwila, WA, United States
Check the event website for more details.