Training Features
The European Database on Medical Devices (EUDAMED)
This training provides practical guidance on EUDAMED registration under the EU MDR and EU IVDR, supporting accurate data entry, regulatory compliance, and device traceability.
Format
E-Learning
Level
Basic
Trainer
Agnieszka Schrieber
Exam
Exam and certificate included
Duration
1 hour
8 modules
Price
€ 170 or equivalent currency
Comprehensive Regulatory Expertise
This training provides a distinct advantage by imparting expertise in navigating EUDAMED, ensuring regulatory compliance, and optimizing transparency in the European medical device market. Participants emerge equipped to seamlessly integrate devices, offering a unique competitive edge.
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
Agnieszka Schrieber
Agnieszka specializes in regulations and technical aspects of medical devices, focusing on Unique Device Identification, GS1 standards, technical documentation, risk management, and global regulatory strategies at Qserve, emphasizing practicality and customer engagement.
