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eu medical device regulations

This class was created by Brainscape user Suzanne Wertz. Visit their profile to learn more about the creator.

By: Suzanne Wertz
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Decks in this class (15)

EMA and Other Regulatory Bodies (Ch. 1)
No deck description has yet been added by the author.
31  cards
History of Regulations (Ch. 2)
No deck description has yet been added by the author.
45  cards
Advertising and Promotion (Ch. 3)
No deck description has yet been added by the author.
35  cards
Enforcement and Competent Authorities (Ch. 4)
No deck description has yet been added by the author.
21  cards
Regulatory Strategy (Ch. 5)
No deck description has yet been added by the author.
13  cards
The New MDR and IVDR (Ch. 6)
No deck description has yet been added by the author.
26  cards
The European Medical Devices Legal System (Ch. 7)
No deck description has yet been added by the author.
82  cards
Medical Devices: Legislation and Classification (Ch. 8)
No deck description has yet been added by the author.
38  cards
In Vitro Diagnostic Medical Devices (Ch. 9)
No deck description has yet been added by the author.
50  cards
General Safety and Performance Requirements and Technical Documentation (Ch. 10)
No deck description has yet been added by the author.
20  cards
Medical Device Preclinical Testing (Ch. 11)
No deck description has yet been added by the author.
10  cards
Clinical Evaluation and Clinical Investigations (Ch. 12)
No deck description has yet been added by the author.
28  cards
Medical Device Conformity Assessment Procedure (Ch. 13)
No deck description has yet been added by the author.
18  cards
Medical Device Compliance: Postmarket Requirements (Ch. 14)
No deck description has yet been added by the author.
21  cards
Combination Products (Ch. 16)
No deck description has yet been added by the author.
3  cards

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eu medical device regulations

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