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Course Name:
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EU-MDR UNDERSTANDING, DOCUMENTING, IMPLEMENTING & MAINTAINING THE QMS
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Course ID:
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1127339 |
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Provider Name:
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QUALITY AND PRODUCTIVITY SOLUTIONS, INC.
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Approved for:
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Description:
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This course is designed to help medical device personnel understand and determine what is required to implement and maintain an EU MDR QMS. Device manufacturers who conduct business in the EU must comply complex Eu-MDR requirements. Students will learn about the new requirements in the MDR, including those related to quality systems, product classification rules, technical documentation, clinical evaluations, Unique Device Identification (UDI), and post market surveillance. Students will learn the following- class discussion on each topic- class exercises practical case studies- homework will be provided to ensure students’ practice. This course can be taken in-person or instructor driven via Zoom. |
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Training Subtype:
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TQM - Total Quality Management
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Location:
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28 Lord Road, Suite 205,
Marlborough, MA 01752
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Program Results In:
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-NA-
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Course Length:
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5 week(s)
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Average No. of Hours/Week:
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7 Hrs
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On-line Course Schedule:
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http://www.qpsinc.com
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Cost/Student:
Includes:
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$3,000.00
Tuition
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Flat Rate Course:
(The cost of this course is based on a flat fee, regardless of the number of employees attending the course)
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No
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Performance Summary
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Program Year (Most Recent):
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