Program Details:

This 2 day class will provide an in-depth look at the key regulatory aspects along with QMS implementation of the European Medical Device Regulations (MDR).  It will be of value to anyone working in the Medical Device community and anyone marketing or planning to market medical devices in Europe. The class will focus on implementation and participants will receive certification of completion, course materials along with a variety of procedure templates and checklists.

The course will be presented over 2 full days. 

Day 1 MDR regulatory aspects including TF/Clinical requirements

Day 2 EU MDR QMS Implementation

Cost: 

2 Day course: $2400.00

Cost includes: lunch and breaks each day as well as course materials.

Registration is limited to 30 people so please register early. 

Course registrations deadline is February 26, 2021.  No refunds after that date.

Room will be of sufficient size to accommodate for Physical Distancing

A signed COVID Waiver will be required of all attendees

The Conference Center (TBD) will have a discount rate for the nights stay. Anyone needing to make reservations can call the hotel and use the code MDR Training

 For further information contact: 

Debbie Iampietro at (508) 259-7374 or debbieiamp@gmail.com

Or Nicohl Asher at Nicohl.Asher@icloud.com