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Medical Devices in Russia, the Ukraine and in the EEC - Marketing authorisation and the medical device approval
Seminar
In Berlin ()
Beschreibung
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Kursart
Seminar
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Dauer
1 Tag
Starting January 2016, common regulations set by the Eurasian Economic Union (EEC) for theregistration of medical devices came into force. And since 2013, a new highly complex law for medical devices was released in Russia.
The aim of the course is to give you a qualified overview of the legislation, different registration strategies in Russia and the EEC member states and how your business might be improved. Learn more about the highest Russian authority Roszdravnadzor and EEC mutual recognition procedure.
A second focus of this course is market access in the Ukraine and the regulation for medical devices. After having attended the course you will know how to currently handle registration and distribution in Russia, Belarus, Kazakhstan and the Ukraine and which legislation changes are still pending.
Hinweise zu diesem Kurs
This unique course addresses the needs of employees in the healthcare industry who intend to register, export, manufacture medical devices to or in Russia, in the EEC and the Ukraine or plan a market access.
Those involved in:
- regulatory and quality affairs
- product management and marketing
- market access and sales
The course is in English.
- export and business development
will particularly benefit from the speakers' first-hand expertise.
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Themen
- Marketing
Inhalte
Medical Devices in Russia, the Ukraine and in the EEC - Marketing authorisation and the medical device approval