Training Features
Products without an intended medical purpose (Annex XVI)
This training is designed to provide actionable insights and practical guidance, helping your organization navigate the regulatory landscape for products without an intended medical purpose (Annex XVI) under the EU MDR, ensuring compliance and proper classification.
Format
E-Learning
Level
Basic
Trainer
Adriana Gavrilciuc
Exam
Exam and certificate included
Duration
3 hours and 30 mins.
9 modules
Price
€ 510 or equivalent currency
Comprehensive Regulatory Expertise
Enroll in this online training on Annex XVI products to gain comprehensive knowledge on regulatory nuances and compliance strategies for non-medical devices under EU regulations.
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.
