FDA Quality System Inspection Technique (QSIT) Audits – Good Preparation Practices

MessageThis Webinar is over
Date Sep 26, 2018
Time 03:00 PM EDT
Cost $13700.00
Large and small medical device companies have a challenge in preparing for and dealing with FDA audits. Quality and Manufacturing personnel in charge of creating and maintaining your quality management system for all of the medical devices manufactured at your facility should be familiar with FDA auditors’ expectations.

This webinar presents important facts to simplify the planning and execution to ensure that the findings by FDA as 483s or as the more serious warning letters are addressed appropriately so your quality system is always audit proof and ready for the QSIT Inspectors.

After having successfully emerged out of a FDA 483 or a warning letter for your medical devices, it is a challenge to maintain the items that you promised to “correct” in your response letter to the FDA as the FDA auditors will dig deep into those items. Hence items that can be scrutinized under a mock QSIT audit by experienced auditors / consultants to confirm your readiness for an unannounced FDA audit will be covered. How to perform a risk-based mock QSIT assessment for your medical device quality system for the key QSIT checklist items will be covered in this webinar.

Areas Covered in the Session :
  • Unique QSIT Subsystems and assessment process
  • Major considerations in the regulatory requirements for:
    • Management Controls
    • Product design Controls
    • Production and Process Controls
    • CAPA Subsystem
    • Sterilization Controls and associated document system controls
  • How to lay a strong foundation for fulfilling FDA’s QSR
  • Latest GMP regulations for medical devices
  • Recent findings by FDA 483s and more serious warning letters
  • Preparing and Executing Audit Proof Quality System
  • Challenges in maintaining the promises made in your response letter to FDA
  • Unannounced FDA audit Readiness
  • How to perform a risk-based mock QSIT assessment
  • Essential components of a well-documented quality system

Who Will Benefit:
A must attend webinar for teams in:
  • Manufacturing Departments
  • Process Engineering
  • Research and Development Departments
  • Design Assurance Departments
  • Quality Assurance Departments
  • Quality Control Departments
  • Quality Engineers
  • CAPA Coordinators
  • Sterilization and Production Cleanroom maintenance Teams
  • Document Control Departments
  • Regulatory Departments


Create your own event
Turn your passion into a business.
Join our mailing list