In-Person Workshop (August 7, 2015)

Reprocessing of Reusable Medical Devices

The patients’ exposure to reusable medical devices is often risky, largely because the quality of reprocessing of these devices is often not up to the mark. FDA is also aware of these risks of infection and has chalked out some strategies to deal with it. This workshop is designed to discuss different aspects of the quality of reprocessing of reusable equipment and how we can reduce the risks involved.

The workshop has an agenda to critically examine various aspects of reprocessing quality and device design. The speaker will discuss various related topics such as validation and reprocessing methodologies, healthcare facility best practices and what measures FDA has taken to address these issues.
Who Will Benefit:
  • Hospitals: Risk Managers, General Supply Managers, Infection Control, Service Managers
  • Gastroenterology Doctors and Nurses
  • Third-party servicer/refurbisher
  • Endoscope specification developer
  • FDA consultants
  • Product liability lawyer
  • Patient advocacy group

    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@fdamap.com