MDR Specialized Course (9th Edition)

MDR Specialized Course (9th Edition)

The live-streamed course is ideal for gaining specific expertise on the European MDR (EU) 2017/745 regulation. The program covers some of the most significant and challenging processes and requirements of the regulation, interpreted alongside the applicable MDCG guidelines. Topics include: manufacturer and other economic operators’ obligations, clinical evaluation, and post-market surveillance. By subscribing to our newsletter, you will have the opportunity to receive more information about the objectives, structure, and content of the training program.

Date

28 May, 2026

Registration Deadline

21 May, 2026

Format

Live streaming

Language

Italian

Price

€2,400 for non Clients
€1,800 for Clients
(VAT excluded)

Download Brochure

The Course includes

Regulatory Affairs Toolkit (experiences, templates, and tools)
Support from an educational tutor
Educational materials
Competency assessments (for each lesson)
Certificate of Competence

Target Audience

Manufacturers
Authorized Representatives
Importers and Distributors
Consultants
PRRC – Art. 15 MDR (EU) 2017/745
Regulatory Affairs Professionals
Quality Management
Quality Assurance
R&D
Other Economic Operators

Certificates and Qualifications

The Course’s program awards a Certificate of Competence
AICQ Sicev Qualification

Benefits

Installment Plans
Option to pay the fee in installments according to an agreed plan.
Career Service
Collaboration with industry partners to create professional opportunities.
Team promotion
10% off for every extra participant from the same organization.