EU MDR: 2017: Online Training

Issued by PathWise

Learners can define key terms used in the EU Medical Device Regulation. They can summarize the responsibilities of important characters in the EU MDR. Learners can identify parts of a Unique Device Identifier. Learners can describe current device classifications and new classification rules.

Type Learning
Level Foundational
Time Hours
Cost Paid

Additional Details

Skills

EU MDR
Medical Device Regulation
Quality Management System

Earning Criteria

Online self led module of training content followed by a test. Learners must pass post course assessment with 80% or higher.

Standards

IACET

PathWise is accredited by the International Association for Continuing Education and Training (IACET). PathWise complies with the ANSI/IACET Standard, which is recognized internationally as a standard of excellence in instructional practices. As a result of this accreditation, PathWise is accredited to issue the IACET CEU.