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EU IVDR Training Courses on the European In Vitro Diagnostic Regulation (2017/746)
EU IVDR Training Courses on the European In Vitro Diagnostic Regulation (2017/746)
Comply Guru offer EU IVDR Training that is available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization learn about new European In Vitro Diagnostic Regulation (2017/746). We were the first training provider to offer Exemplar Global Certified EU IVDR Training in the world...
EU IVDR Training Types
The European In Vitro Diagnostic Regulation (2017/746) is the new legislation applicable to IVD medical devices being placed on the EU market. The IVDR replaces the EU In Vitro Diagnostics Directive (IVDD) 98/79/EC.
Comply Guru offer the following types of EU IVDR training courses depending on the target audience and/or learning objectives, including:
Essentials Training is for non-QARA personnel who need a short, general overview of the EU IVDR (2017/746) for awareness purposes.
Practitioner Training is for those who are new to the Regulation but working in Quality or Regulatory Affairs and need a broad understanding of the EU IVDR (2017/746).
This course takes you through the new , not just from an industry perspective, but also from a Notified Body perspective. It has been specifically designed for Quality & Regulatory Professionals who are new to the Regulation.
This course provides clarity on the role and responsibilities of the Person Responsible for Regulatory Compliance (PRRC) introduced under Article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).
Comply Guru offer a European In Vitro Diagnostic Regulation (EU IVDR 2017/746) Essentials Course for organizations looking for a concise, high-level introduction for their staff.
2 hours Comply Guru
$ 395.00
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