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The Re-Processing Medical Devices conference is about the major developments in policies in reprocessing of single-use medical devices (SUDs) and reusable ones. The health ministries have issued guidance to health care facilities and device manufactures. The surgical instruments also have become complex in use because of the advance in technology. The Re-Processing Medical Devices conference will also touch upon the minimization of risks while using medical instrument. It will teach how to build relationship between vendor and manufacturers.
In the conference, the sessions include the following topics in which the speakers will touch upon:
- Manufacturer validation of reprocessing instructions
- New accreditation standards for hospital reprocessing
- Increasing collaboration between the hospital community and manufacturers
- Manufacturers specifying non-standard sterilization cycles
- New Provincial directives on reuse of SUDs
- Adequate reprocessing instructions from manufacturers
- Impact of improvements on infection rates
- Problems with cleanliness of loaned or leased reusable devices
Visitor Profile
The visitors at the Re-Processing Medical Devices conference are:
- Medical Colleges
- Provincial Health Ministries
- Hospital Presidents
- Infection Control Practitioners
- CFOs
- Risk Managers
- Directors / Managers of Infection Prevention and Control
- Biomedical Engineers
- Chiefs of Staff, Chiefs
- Nurse Managers and Practitioners
- Clinical Care Managers
- Public Policy Analysts
- Clinical Educators
- Medical Device Manufacturing Presidents
- Directors of Emergency Medicine
- Directors of Product Development
- Regulatory Affairs
- Quality and Product Support
- Deputy Ministers of Federal
- Executive Directors of Healthcare Associations
- Advisors
- Researchers
- Partners
- Media
Organizer
Incisive Media Canada, Inc
