Presentations

Medical Device Clinical Studies in Low Resource Settings - FOSEP - University of Washington - 2012- Dave Hammond

Medical Device Regulations in Australia, China and Singapore - University of Washington - PCE - 2011 - Dave Hammond

Home Use Medical Devices and Usability Trials - ACRP - 2011 Dave Hammond & Martha Feldman

Genetic Testing and the Enhancement Clinical Trial Design - ACRP - 2011 - Dave Hammond & Jinling Wei

Regulatory Environments Outside the US - PATH - 2010 - Dave Hammond

Software Validation in the real world - University of Washington, Masters in Health Informatics - 2009 - Sarah Hammond

Verification & Validation of Clinical Data Management Software - University of Washington, Clinical Trials Program - 2009 - Sarah Hammond

The History of Human Subjects Protection & the Code of Federal Regulations – Arizona Cancer Institute, Scottsdale, AZ - 2008 - Dave Hammond

Objective Evaluation of Contract Research Organizations – Providing Appropriate Technologies for Health (PATH) - 2008 - Dave Hammond

Implementing Remote-hosted Document Control Systems for Medical Device Companies – Agility, Las Vegas, NV - 2006 - Dave Hammond

Monitoring clinical studies: the similarities and differences between medical device and drug studies - University of Washington, Biomedical Regulatory Affairs Program - 2003-2008 - Dave Hammond

Preparing Devices for Clinical Studies - University of Washington, Biomedical Regulatory Affairs Program - 2005 - 2008 - Dave Hammond

International Clinical Trials - University of Washington, Biomedical Regulatory Affairs Program - 2008 - Dave Hammond

Monitoring and Medical Devices - RAPS’ Good Clinical Practices Webcast – 2005 - Dave Hammond