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
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Mauris condimentum varius est vitae convallis. Integer vitae magna at nisl aliquet bibendum.
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
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.
