Get specialized training to reprocess reusable medical devices such as surgical tools and patient care equipment.
Get specialized training to reprocess reusable medical devices such as surgical tools and patient care equipment.Graduates of this program are eligible to take the Certified Medical Device Reprocessing Technician (CMDRT) examination from the Canadian Standards Association (CSA).
VCC is an approved training provider for Medical Device Reprocessing Technician through the Canadian Standards Association.
What You Will Learn
Upon completion of this program, graduates will have acquired the knowledge and ability to:
What To Expect
This is a full-time face-to-face program with on-line supported learning. Classes are scheduled Monday to Friday. Hours may vary. The clinical placement may include some evenings.
The program is divided into two components: theory and clinical. Both components are taken simultaneously. The theory component is delivered through classroom instruction, group discussions, case-studies, and simulations.
Students apply theoretical knowledge in the clinical practicum, which takes place in hospital MDR Departments.
Recommended Characteristics
Located in the heart of Vancouver, British Columbia, VCC helps students gain skills and knowledge to make a difference in the world.
Moreover, the MDRT course is instrumental in the healthcare system by training technicians who are paramount in ensuring that medical devices undergo proper decontamination and sterilization processes, thus mitigating the risk of infection transmission through surgical instruments and equipment.
Develop the knowledge and technical skills required for a career as a Medical Device Reprocessing Technician (MDR).
This course covers elements of decontamination, preparation, assembly, sterilization, storage and distribution of instruments and medical devices.
This course introduces students to the key scientific principles and methods of disinfection and sterilization utilized in today's health care settings.
By the end of the course, participants will have a comprehensive understanding of the regulatory requirements for medical devices, including Medical Device Classification and Quality Management, MDSAP, labelling requirements, and the application submission process.
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