Webinar “Fundamentals of conformity assessment for medical devices. Must-have for importer, Authorized Representative, and manufacturer”
Details:
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Date: November 7, 2023
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Time: from 12:00 to 14:00 Kyiv time (GMT +2)
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Event adress: Online
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Language of the event: Ukrainian
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Speakers:
- Viktoriia Moroz, Key Account Manager
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Cost:
- Free, subject to prior registration
In the event:
- What is required to place medical devices on the market and put them into service;
- How the class of the medical device impacts the certification procedure;
- Procedure types: self-declaration, audit, CE recognition, batch certification;
- Other "non-medical" technical regulations that may be applicable to medical devices;
- Authorized representative of the manufacturer in Ukraine: role, duties, responsibilities;
- What documents are required for conformity assessment;
- National documents: labeling, instruction, check-list, declaration;
- Registration of class I and IVD "other";
- Audit and recognition of the CE certificate;
- Market surveillance.
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