Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar by GlobalCompliancePanel 2010

  • 20 Oct 2010
  • Webinar

Description

Supplier qualification and assessment is required in both the QSR regulations and ISO standards.

Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices. Areas Covered in the Session:

  • Regulatory Requirements
  • Key Elements of a Supplier Qualification Program
  • Utilizing Quality Agreements
  • Supplier Assessment
  • Supplier Nonconformance
  • Required Documentation
Who Will Benefit: This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:

  • Purchasing management
  • Regulatory management
  • QA management
  • Consultants

Past Events

Important

Please, check "Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner -Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical laboratories, Medical technology, Pharma

Other Events with Similar Categories

Other Events with Similar Location or Organizer

Featured Conferences & Exhibitions