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
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.
