Comply Guru are the first in the world to offer Multi-Accredited European In Vitro Diagnostic Regulation (IVDR 2017/746) Training with the Regulatory Affairs Professionals Society (RAPS) and Exemplar Global offering credentials for the Medical Device Industry that are globally recognized.
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 different types of EU IVDR training courses depending on the target audience and training needs. We can also tailor training to meet your company’s specific needs or requirements. Our courses are available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization master the European In Vitro Diagnostic Regulation (IVDR 2017/746).
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