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

OVERVIEW Notified bodies and the FDA cannot require your suppliers to meet the quality system regulations, so they must make sure you are exercising sufficient control over those suppliers. You must make sure your supplier management and system meets all required regulations, especially for critical suppliers. Sure, you depend on your suppliers to provide you with goods and services, but can your system prove that you have sufficient control over your suppliers to assure auditors and regulatory agencies that your product is safe and meets all your requirements?

WHY SHOULD YOU ATTEND
This class will review the QSR and ISO requirements for supplier evaluation, including defining the types of suppliers that require evaluation, including “critical” suppliers and outsourced processes. The QSR and ISO requirements for supplier assessment will be defined as well. The webinar will discuss the application of a risk-based process resulting in a customized supplier management system.

AREAS COVERED
Review of FDA and ISO requirements
Types of suppliers that must be qualified
Defining critical suppliers
Classification of suppliers
Outsourced processes
The Quality Agreement
Recommended Practices

LEARNING OBJECTIVES

Review of FDA and ISO requirements
Recommended Practices
How to avoid “Death by Supplier Audit”
Documentation requirements

WHO WILL BENEFIT

Supply chain management
Buyers
Purchasing management
CAPA Coordinators
Regulatory management
QA management
Executive management
Internal auditors

For more detail please click on this below link:
https://bit.ly/2GM9E3m

Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882

Read More

View Less