MedCon 2010 Quality Track Agenda

Quality Track Agenda

Information will be updated as the agenda detail is finalized.

  • Design Controls (validation, change control, design transfer)
  • Process Validation (risk management)
  • Quality Assurance for Combination Products
  • Post Market Surveillance (CAPA, Complaints, Corrections/Recalls)
  • Device Supplier Controls
  • Management Review
  • Preparing for International Inspections/Audits

 

Strategic Committee Member

Monica Wilkins, Abbott LaboratoriesMonica Wilkins

Sr. Director,
Corporate QA and Compliance
Abbott Laboratories
Former FDA National Medical Device Expert

 

Please contact Marla Phillips if you would like to be considered for speaker or moderator opportunities.