Guest Speaker

ASQ, Las Vegas Section:
  • An Effective CAPA System for Medical Device Manufacturers
  • Transitioning from ISO 9001:2008 to ISO 13485:2003–Going After the Medical Device Business
ASQ, Palomar Section (Southern CA):
  • Major, Minor, or Is it Just the Auditor’s Opinion–Writing Clear and Concise Audit Nonconformities (and How to Defend Them)
  • ISO 9001:2015 Roundtable Discussion
  • FDA Inspections vs. Quality System Audits—Know the Differences
MD&M West Conference:
  • CAPA—Common Pitfalls and How to Avoid Them
  • Documentation Management for the Medical Device Industry (co-presenter)
Institute of Validation Technology Medical Device Workshops:
  • Post Market Surveillance: Why Complaints Aren’t (Usually) Enough
Medical Product Development certificate program, UC-Irvine Extension:
  • Quality System Regulations 21 CFR Part 820
Northern California Discussion Group, ASQ Biomedical Division:
  • EN ISO 13485:2003, Process Based Approach
SDRAN Medical Device Conference:
  • Canadian Medical Device Conformity Assessment Systems
SDRAN RAC Study Groups:
  • Medical Device Regulations 21 CFR Part 803, 820