Building a Vendor Qualification Program for FDA Regulated Industries 2016

  • 18-19 Aug 2016
  • Orlando, FL, United States

Description

Topics
  • How change control and other quality programs feed into the vendor qualification program
  • Sustainable structure for a vendor qualification program
  • The best potential vendor and what a potential vendor needs to supply before qualification
  • Usable audit forms/checklists and other vendor qualification program document templates
  • On-site and off-site verifications
  • Vendors that meet your requirements prior to qualification
  • Estimate costs and time associated with vendor qualification
  • Monitor and re-qualify vendors
  • Common pitfalls to avoid when qualifying vendors
  • Respond to customer and regulatory audit observations associated with vendor qualification
Who should Attend
  • Regulators
  • Internal Auditors
  • Compliance Officers
  • Legal Departments
  • QC Managers
  • Purchasing Managers
  • Quality and Sales Department Staff
  • QA Managers
  • Senior Management
  • Compliance Consultants

Past Events

Important

Please, check "Building a Vendor Qualification Program for FDA Regulated Industries" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Management, Quality assurance
Government & Global Issues: Law & Regulations
Science: Life Sciences & Biology

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