Training Features

Introduction to Custom-Made Devices

This training is designed to provide actionable insights and practical guidance, introducing your organization to the regulatory requirements for custom-made devices under the EU MDR, ensuring compliance and tailored product delivery.
Format

E-Learning

Level

Basic

Trainer

Stephanie Valk

Exam

Exam and certificate included

Duration

30 minutes
3 modules

Price

€ 80 or equivalent currency

Comprehensive Regulatory Expertise

Join our online Custom-Made Devices Training to gain expert knowledge on the evolving regulatory landscape of custom-made medical devices, with comprehensive and up-to-date insights to enhance your expertise.
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

Stephanie Valk

Stephanie specializes in PMS Vigilance and brings extensive expertise in Regulatory Affairs and Quality Management Systems, utilizing her pragmatic, pro-active, and result-driven approach to interface with various teams, including management, sales, and supply chain, and has over 12 years of experience in Quality Management Systems, holding a Master's degree in Human Movement Science.