Training Features

Understanding Transitional Provisions

This training provides an overview of the transitional provisions under the MDR, explaining how legacy devices can temporarily remain on the market while meeting defined safety and performance requirements.
Format

E-Learning

Level

Basic

Trainer

Adriana Gavrilciuc

Exam

Exam and certificate included

Duration

45 mins.
6 modules

Price

€ 165 or equivalent currency

Comprehensive Regulatory Expertise

Gain expertise in drafting precise and effective transitional measures with this comprehensive 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

Adriana Gavrilciuc

Adriana brings extensive expertise in Regulatory Affairs, specializing in EU MDR compliance for low to high-risk medical devices, including Technical Documentation setup and review, gap analyses, and training, with a background spanning biopharmaceuticals and medical devices.