EU MDR Training Courses on the European Medical Device Regulation (MDR 2017/745)

Comply Guru are the first in the world to offer Multi-Accredited European Medical Device Regulation (MDR 2017/745) Training with the Chartered Quality Institute (CQI), International Registrar of Certificated Auditors (IRCA) and the Regulatory Affairs Professionals Society (RAPS) offering credentials for the Medical Device Industry that are globally recognized.

The European Medical Device Regulation (MDR 2017/745) has replaced the Medical Devices Directive (93/42/EEC) as the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

Comply Guru offer different types of EU MDR 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 Medical Device Regulation (MDR 2017/745).