Training Features

Responsibilities of Manufacturers and Economic Operators

This training is designed to provide actionable insights and practical guidance, helping your organization understand the responsibilities of manufacturers and economic operators under the EU MDR, ensuring full compliance and streamlined operations.
Format

E-Learning

Level

Basic

Trainer

Agnieszka Schreiber

Exam

Exam and certificate included

Duration

2 hours
5 modules

Price

€ 230 or equivalent currency

Comprehensive Regulatory Expertise

Explore the vital obligations of manufacturers and economic operators in the medical device industry through this virtual training.
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

Agnieszka Schreiber

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.