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Who should attend Best Practices for Lean Supplier Management in Compliance with FDA and ISO 13485 Requirements Webinar
This webinar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program
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Best Practices for Lean Supplier Management in Compliance with FDA and ISO 13485 Requirements Webinar  

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This webinar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program

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Seminar Summary:

This webinar will review in detail the FDA QSR and ISO requirements for supplier evaluation and assessment, and discuss cost effective options for many of the common practices for achieving compliance. (see full course description)

 
 

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Training Course Syllabus:


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

Why Should you Attend

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? Your supplier management program can be in compliance, but is it cost effective? If not, your unquantifiable overhead costs may be out of control. Is your supplier management program collaborative with your suppliers? If your company is too demanding of your suppliers, you risk alienating them or even worse losing them - try explaining that to your supply chain management!

This webinar 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.

Who will Benefit

This webinar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program that is both compliant and cost-efficient. The employees who will benefit include: Supply chain management, Buyers, Purchasing management, CAPA Coordinators, Regulatory management, QA management, Executive management, Internal auditors, Regulatory personnel, Quality Engineering personnel, Sales and Marketing personnel, Customer Service personnel, R&D personnel, Manufacturing Engineering, Consultants, Quality system auditors

Seminar Summary:

This webinar will review in detail the FDA QSR and ISO requirements for supplier evaluation and assessment, and discuss cost effective options for many of the common practices for achieving compliance. (see full course description)

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