Best Practices for Lean Supplier Management in Compliance with FDA and ISO 13485 Requirements

Website https://www.onlinecompliancepanel.com/webinar/Best-Practices-for-Lean-Supplier-Management-in-Complia | Edit Freely

Category Supplier Evaluation and assessment, medical device quality requirements, medical device supplier evaluation, medical device supplier, quality system regulation, ISO 13485 requirements, medical device compliance, FDA medical device requirements, FDA medical device regulations, ISO 13485, device regulations, assessing medical device suppliers, assessing medical device vendors, supplier CAPA, supplier related corrective action

Deadline: December 05, 2017 | Date: December 06, 2017

Venue/Country: Online, U.S.A

Updated: 2017-11-14 21:44:19 (GMT+9)

Call For Papers - CFP

Objectives of the Presentation:

Supplier Selection

Review of FDA and ISO requirements

Types of suppliers that must be qualified

Defining critical suppliers

Outsourced processes

Recommended Practices

Supplier Assessment

Review of FDA and ISO requirements

Recommended practices

Justification of desktop audits

Documentation requirements

For Registration:

https://www.onlinecompliancepanel.com/webinar/Best-Practices-for-Lean-Supplier-Management-in-Compliance-with-FDA-and-ISO-13485-Requirements-505073/DECEMBER-2017-ES-OURGLOCAL

Website:https://www.onlinecompliancepanel.com/home

Note: Use Promo Code HYED6Z and get 10% off on registration (Valid till DECEMBER 31st 2017)