Training Features

Medical Device Consultant in Germany and Austria

This training provides an in-depth introduction to the legal responsibilities, regulatory requirements, and essential skills needed for consultants to ensure compliance and effective support in clinical settings within Germany and Austria.
Format

E-Learning

Level

Basic

Trainer

Robert Paassen

Exam

Exam and certificate included

Duration

3 hours and 30 mins.
13 modules

Price

€ 510 or equivalent currency

Comprehensive Regulatory Expertise

Uncover the latest strategies and regulatory insights essential for maintaining medical device safety and performance. Join us to refine your compliance with Medical Device Consultant requirements in Germany and Austria.
Upon successful completion of the program, participants receive a recognized certification, boosting their career prospects and demonstrating their expertise to employers and clients.

Certification and Career Advancement

We offer a flexible learning schedule, allowing professionals to balance their training with their busy work and personal lives, ensuring accessibility to a wide range of learners.

Flexible Learning Schedule

Modules

Explore the training modules available in this course

Meet the Trainer

Robert Paassen

Robert Paassen is a Regulatory Affairs & Quality Assurance consultant specializing in EU MDR, serving as a Startup Lead, with expertise in clinical evaluations, quality management system remediation, CAPA management, risk management, and supporting audits.