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Medical_Device_HQ
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FEED
42
CONTRIBUTION
42
FAVORITES
Videos
42
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by time
06:08
How much does a clinical investigation cost
34
6-14
28:39
Short course on SaMD (Software as a medical device)
95
6-3
11:46
Conformity assessment procedures for medical device manufacturers
43
5-28
06:38
What is good clinical practice (GCP)
5
5-13
12:34
Documenting compliance with IEC 62304 in medical device software development
25
5-9
18:34
How to perform the summative evaluation for medical devices (IEC 62366-1)
173
4-8
15:30
Short course on Usability Engineering for Medical Devices and IEC 62366-1
2
4-3
21:40
Post-market surveillance as a medical device requirement in the EU
476
3-12
07:34
Authorised representatives, importers and distributors under the MDR
146
3-8
17:39
Medical Device Regulation codes
49
3-4
19:25
Short course on Clinical Investigation for Medical Devices and ISO 14155
173
3-1
12:36
UDI requirements for medical device manufacturers in the EU
127
2-26
14:54
Short course on the Medical Device Regulation (EU) 2017_745
145
2-19
07:26
How to work with medical device risk management
52
2-2
14:56
Risk control measures in medical device software
7
1-22
03:59
The responsibilities of a clinical investigation sponsor
52
1-19
09:31
System, item and units in medical device software
20
1-15
14:22
What is a medical device according to the MDR
43
1-8
06:43
What are the major changes in ISO 14155 2020
76
1-5
08:40
Managing and documenting SOUP and OTS in medical device software
24
1-2
1
2
3
42 results
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