FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS 2018

  • 10 Aug 2018
  • Webinar

Description

FDA Compliant QC and QA Practices Creating a Perfect, Audit-Ready QMS 2018 is a webinar that covers topics such as:

  • Review the roles of Quality Control and Quality Assurance in your facility
  • Discover FDA expectations for Quality Control and Quality Assurance
  • Identify the requirements for a Sound QMS
  • Learn how to avoid receiving 483s for Quality Control and Quality Assurance issues
  • Learn how to implement an effective audit ready QMS
  • Recognize how to implement and apply GMP concepts to your Quality Control and Quality Assurance roles

FDA Compliant QC and QA Practices Creating a Perfect, Audit-Ready QMS 2018 is intended for:

  • Quality Control Departments
  • Research and Development Departments
  • Validation Professionals
  • Quality Assurance Departments
  • Regulatory Departments
  • Management and Supervisory Personnel

Past Events

Important

Please, check "FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Internal Audit & Compliance, Management, Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma

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