27th & 28th November 2018
Radisson Blu Plaza Hotel Ljubljana (Slovenian language)
Regulatory seminar and workshop on medical devices
NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU – Why to review current agreements?
The new legislation on medical devices is adopted, and the transitional period for its implementation is slowly running out. Distributors of medical devices will have to harmonize their business with new requirements. Therefore, it is necessary not only to become acquainted with changes and their potential impact on business, but also to prevent surprises in practice due to overlooked details, different interpretation of requirements or methods of their fulfillment. Sometimes this is an existential importance for the company. In particular, it is a sensitive area of a new division of responsibility in relation to manufacturers of medical devices, authorized representatives, importers or users.
The seminar and the workshop are originally intended for distributors of medical devices, but they are suitable and useful for all other business entities as well, since the changes also affect their business.
Click HERE for more information about seminar and workshop.
Click HERE to apply for seminar and workshop.